CA2959695A1 - Substrats contenant des compositions reduisant les mauvaises odeurs - Google Patents

Substrats contenant des compositions reduisant les mauvaises odeurs Download PDF

Info

Publication number: CA2959695A1
Authority: CA; Canada
Prior art keywords: methyl; dimethyl; acetate; isopropyl; ethyl
Prior art date: 2014-09-26
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Abandoned

Application number

CA2959695A

Other languages

English (en)

Inventor

Gayle Marie Frankenbach

Judith Ann Hollingshead

Steven Anthony Horenziak

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Procter and Gamble Co

Original Assignee

Procter and Gamble Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2014-09-26

Filing date

2015-09-25

Publication date

2016-03-31

2015-09-25 Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co

2016-03-31 Publication of CA2959695A1 publication Critical patent/CA2959695A1/fr

Status Abandoned legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 153
230000009467 reduction Effects 0.000 title claims abstract description 81
239000000758 substrate Substances 0.000 title claims abstract description 41
238000000034 method Methods 0.000 claims abstract description 23
239000000463 material Substances 0.000 claims description 146
239000004744 fabric Substances 0.000 claims description 118
-1 (1Z,5Z)-1,5-dimethyl-8-(propan-ylidene)cyclodeca-1,5-diene Chemical compound 0.000 claims description 91
235000014113 dietary fatty acids Nutrition 0.000 claims description 78
239000000194 fatty acid Substances 0.000 claims description 78
229930195729 fatty acid Natural products 0.000 claims description 78
239000003795 chemical substances by application Substances 0.000 claims description 31
JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims description 29
239000002304 perfume Substances 0.000 claims description 29
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 28
229920000642 polymer Polymers 0.000 claims description 24
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 21
150000001412 amines Chemical class 0.000 claims description 18
229920000098 polyolefin Polymers 0.000 claims description 18
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 16
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 14
229910052740 iodine Inorganic materials 0.000 claims description 14
239000011630 iodine Substances 0.000 claims description 14
NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 claims description 13
MMXKVMNBHPAILY-UHFFFAOYSA-N ethyl laurate Chemical compound CCCCCCCCCCCC(=O)OCC MMXKVMNBHPAILY-UHFFFAOYSA-N 0.000 claims description 13
IHPKGUQCSIINRJ-CSKARUKUSA-N (E)-beta-ocimene Chemical compound CC(C)=CC\C=C(/C)C=C IHPKGUQCSIINRJ-CSKARUKUSA-N 0.000 claims description 12
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 12
FLIACVVOZYBSBS-UHFFFAOYSA-N Methyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC FLIACVVOZYBSBS-UHFFFAOYSA-N 0.000 claims description 12
NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 claims description 12
150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 12
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 11
239000003205 fragrance Substances 0.000 claims description 11
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims description 10
239000004927 clay Substances 0.000 claims description 10
KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 claims description 10
WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 claims description 10
KMPQYAYAQWNLME-UHFFFAOYSA-N undecanal Chemical compound CCCCCCCCCCC=O KMPQYAYAQWNLME-UHFFFAOYSA-N 0.000 claims description 10
CRDAMVZIKSXKFV-YFVJMOTDSA-N (2-trans,6-trans)-farnesol Chemical compound CC(C)=CCC\C(C)=C\CC\C(C)=C\CO CRDAMVZIKSXKFV-YFVJMOTDSA-N 0.000 claims description 9
WMOPMQRJLLIEJV-DOMZBBRYSA-N 10-epi-eudesm-4-en-11-ol Chemical compound C1[C@H](C(C)(C)O)CC[C@]2(C)CCCC(C)=C21 WMOPMQRJLLIEJV-DOMZBBRYSA-N 0.000 claims description 9
GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 claims description 9
MQWIFDHBNGIVPO-KYOSRNDESA-N valerianol Chemical compound C1C[C@@H](C(C)(C)O)C[C@@]2(C)[C@H](C)CCC=C21 MQWIFDHBNGIVPO-KYOSRNDESA-N 0.000 claims description 9
DYLPEFGBWGEFBB-OSFYFWSMSA-N (+)-β-cedrene Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1C(=C)CC2 DYLPEFGBWGEFBB-OSFYFWSMSA-N 0.000 claims description 8
NFLGAXVYCFJBMK-IUCAKERBSA-N (-)-isomenthone Chemical compound CC(C)[C@@H]1CC[C@H](C)CC1=O NFLGAXVYCFJBMK-IUCAKERBSA-N 0.000 claims description 8
IHPKGUQCSIINRJ-NTMALXAHSA-N (Z)-beta-ocimene Chemical compound CC(C)=CC\C=C(\C)C=C IHPKGUQCSIINRJ-NTMALXAHSA-N 0.000 claims description 8
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 8
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 8
UAVFEMBKDRODDE-UHFFFAOYSA-N Vetiveryl acetate Chemical compound CC1CC(OC(C)=O)C=C(C)C2CC(=C(C)C)CC12 UAVFEMBKDRODDE-UHFFFAOYSA-N 0.000 claims description 8
QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 claims description 8
HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 claims description 8
239000000975 dye Substances 0.000 claims description 8
239000002979 fabric softener Substances 0.000 claims description 8
239000004615 ingredient Substances 0.000 claims description 8
239000004094 surface-active agent Substances 0.000 claims description 8
NNWHUJCUHAELCL-SNAWJCMRSA-N trans-isomethyleugenol Chemical compound COC1=CC=C(\C=C\C)C=C1OC NNWHUJCUHAELCL-SNAWJCMRSA-N 0.000 claims description 8
ZLQADKTVJQXDIG-UHFFFAOYSA-N α-agarofuran Chemical compound C1CC(C2)C(C)(C)OC22C(C)=CCCC21C ZLQADKTVJQXDIG-UHFFFAOYSA-N 0.000 claims description 8
WMOPMQRJLLIEJV-IUODEOHRSA-N (+)-gamma-eudesmol Chemical compound C1[C@H](C(C)(C)O)CC[C@@]2(C)CCCC(C)=C21 WMOPMQRJLLIEJV-IUODEOHRSA-N 0.000 claims description 7
XCPQUQHBVVXMRQ-UHFFFAOYSA-N (-)-7,7-Dimethyl-2-methylenebicyclo[2.2.1]heptane Chemical compound C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 claims description 7
SPCXZDDGSGTVAW-XIDUGBJDSA-N (-)-alpha-gurjunene Chemical compound C[C@@H]1CC[C@H]2C(C)(C)[C@H]2C2=C(C)CC[C@H]12 SPCXZDDGSGTVAW-XIDUGBJDSA-N 0.000 claims description 7
HICAMHOOTMOHPA-HIFRSBDPSA-N (5r,6r)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-5,7-dihydro-4h-1-benzofuran Chemical compound C1[C@@](C=C)(C)[C@@H](C(=C)C)CC2=C1OC=C2C HICAMHOOTMOHPA-HIFRSBDPSA-N 0.000 claims description 7
OFHHDSQXFXLTKC-UHFFFAOYSA-N 10-undecenal Chemical compound C=CCCCCCCCCC=O OFHHDSQXFXLTKC-UHFFFAOYSA-N 0.000 claims description 7
LOKPJYNMYCVCRM-UHFFFAOYSA-N 16-Hexadecanolide Chemical compound O=C1CCCCCCCCCCCCCCCO1 LOKPJYNMYCVCRM-UHFFFAOYSA-N 0.000 claims description 7
ZITVKGIRQCDOSX-UHFFFAOYSA-N 1h-cyclopropa[a]naphthalene Chemical compound C1=CC=CC2=C3CC3=CC=C21 ZITVKGIRQCDOSX-UHFFFAOYSA-N 0.000 claims description 7
JRTBBCBDKSRRCY-UHFFFAOYSA-N 3,7-dimethyloct-6-en-3-ol Chemical compound CCC(C)(O)CCC=C(C)C JRTBBCBDKSRRCY-UHFFFAOYSA-N 0.000 claims description 7
WRYLYDPHFGVWKC-UHFFFAOYSA-N 4-terpineol Chemical compound CC(C)C1(O)CCC(C)=CC1 WRYLYDPHFGVWKC-UHFFFAOYSA-N 0.000 claims description 7
FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 claims description 7
VZWGRQBCURJOMT-UHFFFAOYSA-N Dodecyl acetate Chemical compound CCCCCCCCCCCCOC(C)=O VZWGRQBCURJOMT-UHFFFAOYSA-N 0.000 claims description 7
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 7
UXAIJXIHZDZMSK-FOWTUZBSSA-N Geranyl phenylacetate Chemical compound CC(C)=CCC\C(C)=C\COC(=O)CC1=CC=CC=C1 UXAIJXIHZDZMSK-FOWTUZBSSA-N 0.000 claims description 7
UUGLJVMIFJNVFH-UHFFFAOYSA-N Hexyl benzoate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1 UUGLJVMIFJNVFH-UHFFFAOYSA-N 0.000 claims description 7
GLZPCOQZEFWAFX-UHFFFAOYSA-N KU0063794 Natural products CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 claims description 7
HPEUJPJOZXNMSJ-UHFFFAOYSA-N Methyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 claims description 7
ZOZIRNMDEZKZHM-UHFFFAOYSA-N Phenethyl phenylacetate Chemical compound C=1C=CC=CC=1CCOC(=O)CC1=CC=CC=C1 ZOZIRNMDEZKZHM-UHFFFAOYSA-N 0.000 claims description 7
LSQXNMXDFRRDSJ-UHFFFAOYSA-N Thymol methyl ether Chemical compound COC1=CC(C)=CC=C1C(C)C LSQXNMXDFRRDSJ-UHFFFAOYSA-N 0.000 claims description 7
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 7
SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 claims description 7
CRPUJAZIXJMDBK-UHFFFAOYSA-N camphene Chemical compound C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 claims description 7
SVURIXNDRWRAFU-OGMFBOKVSA-N cedrol Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1[C@@](O)(C)CC2 SVURIXNDRWRAFU-OGMFBOKVSA-N 0.000 claims description 7
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 claims description 7
RGXWDWUGBIJHDO-UHFFFAOYSA-N ethyl decanoate Chemical compound CCCCCCCCCC(=O)OCC RGXWDWUGBIJHDO-UHFFFAOYSA-N 0.000 claims description 7
XIRNKXNNONJFQO-UHFFFAOYSA-N ethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC XIRNKXNNONJFQO-UHFFFAOYSA-N 0.000 claims description 7
MMKRHZKQPFCLLS-UHFFFAOYSA-N ethyl myristate Chemical compound CCCCCCCCCCCCCC(=O)OCC MMKRHZKQPFCLLS-UHFFFAOYSA-N 0.000 claims description 7
BYEVBITUADOIGY-UHFFFAOYSA-N ethyl nonanoate Chemical compound CCCCCCCCC(=O)OCC BYEVBITUADOIGY-UHFFFAOYSA-N 0.000 claims description 7
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 claims description 7
NCDCLPBOMHPFCV-UHFFFAOYSA-N hexyl hexanoate Chemical compound CCCCCCOC(=O)CCCCC NCDCLPBOMHPFCV-UHFFFAOYSA-N 0.000 claims description 7
PBGWNXWNCSSXCO-UHFFFAOYSA-N hexyl octanoate Chemical compound CCCCCCCC(=O)OCCCCCC PBGWNXWNCSSXCO-UHFFFAOYSA-N 0.000 claims description 7
CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 claims description 7
ZAZKJZBWRNNLDS-UHFFFAOYSA-N methyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OC ZAZKJZBWRNNLDS-UHFFFAOYSA-N 0.000 claims description 7
ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 claims description 7
VKCYHJWLYTUGCC-UHFFFAOYSA-N nonan-2-one Chemical compound CCCCCCCC(C)=O VKCYHJWLYTUGCC-UHFFFAOYSA-N 0.000 claims description 7
YLYBTZIQSIBWLI-UHFFFAOYSA-N octyl acetate Chemical compound CCCCCCCCOC(C)=O YLYBTZIQSIBWLI-UHFFFAOYSA-N 0.000 claims description 7
OSORMYZMWHVFOZ-UHFFFAOYSA-N phenethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCC1=CC=CC=C1 OSORMYZMWHVFOZ-UHFFFAOYSA-N 0.000 claims description 7
FRMCCTDTYSRUBE-BGPZULBFSA-N spathulenol Chemical compound C1CC(=C)[C@@H]2CC[C@](C)(O)[C@H]2[C@@H]2C(C)(C)[C@@H]21 FRMCCTDTYSRUBE-BGPZULBFSA-N 0.000 claims description 7
UHUFTBALEZWWIH-UHFFFAOYSA-N tetradecanal Chemical compound CCCCCCCCCCCCCC=O UHUFTBALEZWWIH-UHFFFAOYSA-N 0.000 claims description 7
QRPLZGZHJABGRS-UHFFFAOYSA-N xi-5-Dodecanolide Chemical compound CCCCCCCC1CCCC(=O)O1 QRPLZGZHJABGRS-UHFFFAOYSA-N 0.000 claims description 7
PHXATPHONSXBIL-UHFFFAOYSA-N xi-gamma-Undecalactone Chemical compound CCCCCCCC1CCC(=O)O1 PHXATPHONSXBIL-UHFFFAOYSA-N 0.000 claims description 7
FCSRUSQUAVXUKK-VNHYZAJKSA-N α-Eudesmol Chemical compound C1C[C@@H](C(C)(C)O)C[C@H]2C(C)=CCC[C@@]21C FCSRUSQUAVXUKK-VNHYZAJKSA-N 0.000 claims description 7
WTOYNNBCKUYIKC-JMSVASOKSA-N (+)-nootkatone Chemical compound C1C[C@@H](C(C)=C)C[C@@]2(C)[C@H](C)CC(=O)C=C21 WTOYNNBCKUYIKC-JMSVASOKSA-N 0.000 claims description 6
QMAYBMKBYCGXDH-SOUVJXGZSA-N (-)-alpha-amorphene Chemical compound C1CC(C)=C[C@@H]2[C@H](C(C)C)CC=C(C)[C@@H]21 QMAYBMKBYCGXDH-SOUVJXGZSA-N 0.000 claims description 6
239000000260 (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol Substances 0.000 claims description 6
ANPXCNWSCGYEMA-UHFFFAOYSA-N (7,7,8,8-tetramethyloctahydro-2,3b-methanocyclopenta[1,3]cyclopropa[1,2]benzen-4-yl)methyl acetate Chemical compound CC1(C)C23C(COC(=O)C)CCC(C)(C)C43C2CC1C4 ANPXCNWSCGYEMA-UHFFFAOYSA-N 0.000 claims description 6
CWRKZMLUDFBPAO-VOTSOKGWSA-N (e)-dec-4-enal Chemical compound CCCCC\C=C\CCC=O CWRKZMLUDFBPAO-VOTSOKGWSA-N 0.000 claims description 6
RTIYSHLNESDZSF-UHFFFAOYSA-N 1-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)-7-oxabicyclo[3.2.1]octane Chemical compound CC1(C)C(C)=CCC1C1(CCC2)CC2(C)OC1 RTIYSHLNESDZSF-UHFFFAOYSA-N 0.000 claims description 6
LJSJTXAZFHYHMM-UHFFFAOYSA-N 7-methyloctyl acetate Chemical compound CC(C)CCCCCCOC(C)=O LJSJTXAZFHYHMM-UHFFFAOYSA-N 0.000 claims description 6
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 6
150000002194 fatty esters Chemical class 0.000 claims description 6
HRGPYCVTDOECMG-RHBQXOTJSA-N methyl cedryl ether Chemical compound C1[C@@]23[C@H](C)CC[C@H]2C(C)(C)[C@]1([H])[C@@](OC)(C)CC3 HRGPYCVTDOECMG-RHBQXOTJSA-N 0.000 claims description 6
239000002904 solvent Substances 0.000 claims description 6
KYWIYKKSMDLRDC-UHFFFAOYSA-N undecan-2-one Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 claims description 6
XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 claims description 5
DAWDTDPJINNEJM-UHFFFAOYSA-N (2,4a,5,8a-tetramethyl-1,2,3,4,7,8-hexahydronaphthalen-1-yl) formate Chemical compound CC1=CCCC2(C)C(OC=O)C(C)CCC21C DAWDTDPJINNEJM-UHFFFAOYSA-N 0.000 claims description 5
YTHRBOFHFYZBRJ-UHFFFAOYSA-N (2-methyl-5-prop-1-en-2-yl-1-cyclohex-2-enyl) acetate Chemical compound CC(=O)OC1CC(C(C)=C)CC=C1C YTHRBOFHFYZBRJ-UHFFFAOYSA-N 0.000 claims description 5
LAEIZWJAQRGPDA-CIRFHOKZSA-N (4ar,6as,10as,10br)-3,4a,7,7,10a-pentamethyl-1,5,6,6a,8,9,10,10b-octahydrobenzo[f]chromene Chemical compound CC1(C)CCC[C@]2(C)[C@H]3CC=C(C)O[C@]3(C)CC[C@H]21 LAEIZWJAQRGPDA-CIRFHOKZSA-N 0.000 claims description 5
KRLBLPBPZSSIGH-CSKARUKUSA-N (6e)-3,7-dimethylnona-1,6-dien-3-ol Chemical compound CC\C(C)=C\CCC(C)(O)C=C KRLBLPBPZSSIGH-CSKARUKUSA-N 0.000 claims description 5
GLZPCOQZEFWAFX-JXMROGBWSA-N (E)-Geraniol Chemical compound CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 claims description 5
CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Chemical compound CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 claims description 5
GLZPCOQZEFWAFX-YFHOEESVSA-N (Z)-Geraniol Chemical compound CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 claims description 5
QELCXXZZKSRBET-PKNBQFBNSA-N (e)-3-methyl-5-phenylpent-2-enenitrile Chemical compound N#C\C=C(/C)CCC1=CC=CC=C1 QELCXXZZKSRBET-PKNBQFBNSA-N 0.000 claims description 5
XXNCXSHVDVCRKB-UHFFFAOYSA-N 1,1-dimethoxycyclododecane Chemical compound COC1(OC)CCCCCCCCCCC1 XXNCXSHVDVCRKB-UHFFFAOYSA-N 0.000 claims description 5
YBUIAJZFOGJGLJ-SWRJLBSHSA-N 1-cedr-8-en-9-ylethanone Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1C(C)=C(C(C)=O)C2 YBUIAJZFOGJGLJ-SWRJLBSHSA-N 0.000 claims description 5
NLWCWEGVNJVLAX-UHFFFAOYSA-N 1-methoxy-2-phenylbenzene Chemical group COC1=CC=CC=C1C1=CC=CC=C1 NLWCWEGVNJVLAX-UHFFFAOYSA-N 0.000 claims description 5
LBICMZLDYMBIGA-UHFFFAOYSA-N 2-methyldecanal Chemical compound CCCCCCCCC(C)C=O LBICMZLDYMBIGA-UHFFFAOYSA-N 0.000 claims description 5
NFAVNWJJYQAGNB-UHFFFAOYSA-N 2-methylundecanal Chemical compound CCCCCCCCCC(C)C=O NFAVNWJJYQAGNB-UHFFFAOYSA-N 0.000 claims description 5
NGDNVOAEIVQRFH-UHFFFAOYSA-N 2-nonanol Chemical compound CCCCCCCC(C)O NGDNVOAEIVQRFH-UHFFFAOYSA-N 0.000 claims description 5
IEODHCKRVCQYNH-UHFFFAOYSA-N 3,5,10,10-tetramethylspiro[5.5]undec-3-en-11-one Chemical compound CC1C=C(C)CCC11C(=O)C(C)(C)CCC1 IEODHCKRVCQYNH-UHFFFAOYSA-N 0.000 claims description 5
PRNCMAKCNVRZFX-UHFFFAOYSA-N 3,7-dimethyloctan-1-ol Chemical compound CC(C)CCCC(C)CCO PRNCMAKCNVRZFX-UHFFFAOYSA-N 0.000 claims description 5
ITJHALDCYCTNNJ-UHFFFAOYSA-N 3-(2-ethylphenyl)-2,2-dimethylpropanal Chemical compound CCC1=CC=CC=C1CC(C)(C)C=O ITJHALDCYCTNNJ-UHFFFAOYSA-N 0.000 claims description 5
XKWSWANXMRXDES-UHFFFAOYSA-N 3-methylbutyl octanoate Chemical compound CCCCCCCC(=O)OCCC(C)C XKWSWANXMRXDES-UHFFFAOYSA-N 0.000 claims description 5
VCYWCSZLXMMLLE-UHFFFAOYSA-N 4-Methoxybenzyl phenylacetate Chemical compound C1=CC(OC)=CC=C1COC(=O)CC1=CC=CC=C1 VCYWCSZLXMMLLE-UHFFFAOYSA-N 0.000 claims description 5
MBZRJSQZCBXRGK-UHFFFAOYSA-N 4-tert-Butylcyclohexyl acetate Chemical compound CC(=O)OC1CCC(C(C)(C)C)CC1 MBZRJSQZCBXRGK-UHFFFAOYSA-N 0.000 claims description 5
FCSRUSQUAVXUKK-KCQAQPDRSA-N 7-epi-alpha-eudesmol Chemical compound C1C[C@H](C(C)(C)O)C[C@H]2C(C)=CCC[C@@]21C FCSRUSQUAVXUKK-KCQAQPDRSA-N 0.000 claims description 5
HVJKZICIMIWFCP-UHFFFAOYSA-N Benzyl 3-methylbutanoate Chemical compound CC(C)CC(=O)OCC1=CC=CC=C1 HVJKZICIMIWFCP-UHFFFAOYSA-N 0.000 claims description 5
ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 claims description 5
NVEQFIOZRFFVFW-UHFFFAOYSA-N Caryophyllene epoxide Chemical compound C=C1CCC2OC2(C)CCC2C(C)(C)CC21 NVEQFIOZRFFVFW-UHFFFAOYSA-N 0.000 claims description 5
HQKQRXZEXPXXIG-DTWJZALFSA-N Cedryl acetate Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1[C@@](OC(C)=O)(C)CC2 HQKQRXZEXPXXIG-DTWJZALFSA-N 0.000 claims description 5
GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 claims description 5
BQOFWKZOCNGFEC-UHFFFAOYSA-N Delta3-Carene Natural products C1C(C)=CCC2C(C)(C)C12 BQOFWKZOCNGFEC-UHFFFAOYSA-N 0.000 claims description 5
VXCUURYYWGCLIH-UHFFFAOYSA-N Dodecanenitrile Chemical compound CCCCCCCCCCCC#N VXCUURYYWGCLIH-UHFFFAOYSA-N 0.000 claims description 5
ZFMSMUAANRJZFM-UHFFFAOYSA-N Estragole Chemical compound COC1=CC=C(CC=C)C=C1 ZFMSMUAANRJZFM-UHFFFAOYSA-N 0.000 claims description 5
URVNHQCLMBMWIW-UHFFFAOYSA-N beta-Terpinyl acetate Chemical compound CC(=C)C1CCC(C)(OC(C)=O)CC1 URVNHQCLMBMWIW-UHFFFAOYSA-N 0.000 claims description 5
UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 claims description 5
229930003633 citronellal Natural products 0.000 claims description 5
235000000983 citronellal Nutrition 0.000 claims description 5
OSOIQJGOYGSIMF-UHFFFAOYSA-N cyclopentadecanone Chemical compound O=C1CCCCCCCCCCCCCC1 OSOIQJGOYGSIMF-UHFFFAOYSA-N 0.000 claims description 5
MXDMETWAEGIFOE-CABCVRRESA-N delta-elemene Chemical compound CC(C)C1=C[C@H](C(C)=C)[C@@](C)(C=C)CC1 MXDMETWAEGIFOE-CABCVRRESA-N 0.000 claims description 5
239000002270 dispersing agent Substances 0.000 claims description 5
LMEAWIUATHINAJ-UHFFFAOYSA-N ethyl (2,3,6-trimethylcyclohexyl) carbonate Chemical compound CCOC(=O)OC1C(C)CCC(C)C1C LMEAWIUATHINAJ-UHFFFAOYSA-N 0.000 claims description 5
YYZUSRORWSJGET-UHFFFAOYSA-N ethyl octanoate Chemical compound CCCCCCCC(=O)OCC YYZUSRORWSJGET-UHFFFAOYSA-N 0.000 claims description 5
RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 claims description 5
ZKKBZSOYCMSYRW-UHFFFAOYSA-N gamma-Terpinyl acetate Chemical compound CC(C)=C1CCC(C)(OC(C)=O)CC1 ZKKBZSOYCMSYRW-UHFFFAOYSA-N 0.000 claims description 5
PHXATPHONSXBIL-JTQLQIEISA-N gamma-undecanolactone Chemical compound CCCCCCC[C@H]1CCC(=O)O1 PHXATPHONSXBIL-JTQLQIEISA-N 0.000 claims description 5
XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 claims description 5
GJQIMXVRFNLMTB-UHFFFAOYSA-N nonyl acetate Chemical compound CCCCCCCCCOC(C)=O GJQIMXVRFNLMTB-UHFFFAOYSA-N 0.000 claims description 5
HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 claims description 5
GGHMUJBZYLPWFD-CUZKYEQNSA-N patchouli alcohol Chemical compound C1C[C@]2(C)[C@@]3(O)CC[C@H](C)[C@@H]2C[C@@H]1C3(C)C GGHMUJBZYLPWFD-CUZKYEQNSA-N 0.000 claims description 5
RUMOYJJNUMEFDD-UHFFFAOYSA-N perillyl aldehyde Chemical compound CC(=C)C1CCC(C=O)=CC1 RUMOYJJNUMEFDD-UHFFFAOYSA-N 0.000 claims description 5
MDHYEMXUFSJLGV-UHFFFAOYSA-N phenethyl acetate Chemical compound CC(=O)OCCC1=CC=CC=C1 MDHYEMXUFSJLGV-UHFFFAOYSA-N 0.000 claims description 5
GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 claims description 5
MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 claims description 5
WJUFSDZVCOTFON-UHFFFAOYSA-N veratraldehyde Chemical compound COC1=CC=C(C=O)C=C1OC WJUFSDZVCOTFON-UHFFFAOYSA-N 0.000 claims description 5
YOVSPTNQHMDJAG-QLFBSQMISA-N β-eudesmene Chemical compound C1CCC(=C)[C@@H]2C[C@H](C(=C)C)CC[C@]21C YOVSPTNQHMDJAG-QLFBSQMISA-N 0.000 claims description 5
WTARULDDTDQWMU-UHFFFAOYSA-N β-pinene Chemical compound C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 claims description 5
QEBNYNLSCGVZOH-NFAWXSAZSA-N (+)-valencene Chemical compound C1C[C@@H](C(C)=C)C[C@@]2(C)[C@H](C)CCC=C21 QEBNYNLSCGVZOH-NFAWXSAZSA-N 0.000 claims description 4
GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 claims description 4
CSKINCSXMLCMAR-RWSFTLGLSA-N (1R,5S,8R)-1,5,11,11-tetramethyltricyclo[6.2.1.02,6]undec-2(6)-ene Chemical compound C[C@H]1CCC=2[C@@]3(CC[C@H](CC1=2)C3(C)C)C CSKINCSXMLCMAR-RWSFTLGLSA-N 0.000 claims description 4
YJVLDTISLGRQTJ-KPFXUCSBSA-N (1R,8R,10S,13R)-5,5,7,9,9,13-hexamethyl-4,6-dioxatetracyclo[6.5.1.01,10.03,7]tetradecane Chemical compound C1[C@@]23[C@H](C)CC[C@H]2C(C)(C)[C@]1([H])C1(C)OC(C)(C)OC1C3 YJVLDTISLGRQTJ-KPFXUCSBSA-N 0.000 claims description 4
DUYRYUZIBGFLDD-AAVRWANBSA-N (1r,3ar,4r,7r)-1,4-dimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,6,7-octahydroazulene Chemical compound C[C@@H]1CC[C@@H](C(C)=C)C=C2[C@H](C)CC[C@@H]21 DUYRYUZIBGFLDD-AAVRWANBSA-N 0.000 claims description 4
GIBQERSGRNPMEH-RYUDHWBXSA-N (1s,4s)-1,4-dimethyl-7-propan-2-ylidene-2,3,4,5,6,8-hexahydro-1h-azulene Chemical compound C1([C@H](CCC(C2)=C(C)C)C)=C2[C@@H](C)CC1 GIBQERSGRNPMEH-RYUDHWBXSA-N 0.000 claims description 4
MMFCJPPRCYDLLZ-CMDGGOBGSA-N (2E)-dec-2-enal Chemical compound CCCCCCC\C=C\C=O MMFCJPPRCYDLLZ-CMDGGOBGSA-N 0.000 claims description 4
239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 claims description 4
SJFICIAGRWSYBO-UHFFFAOYSA-N (7,7,8,8-tetramethyloctahydro-2,3b-methanocyclopenta[1,3]cyclopropa[1,2]benzen-4-yl)methanol Chemical compound C1C2C3(C(CCC4CO)(C)C)C42C(C)(C)C1C3 SJFICIAGRWSYBO-UHFFFAOYSA-N 0.000 claims description 4
CDOSHBSSFJOMGT-SNVBAGLBSA-N (S)-linalool Chemical compound CC(C)=CCC[C@](C)(O)C=C CDOSHBSSFJOMGT-SNVBAGLBSA-N 0.000 claims description 4
MMCDSVCBSAMNPL-HJWRWDBZSA-N (Z)-4-Dodecenal Chemical compound CCCCCCC\C=C/CCC=O MMCDSVCBSAMNPL-HJWRWDBZSA-N 0.000 claims description 4
NVIPUOMWGQAOIT-RQOWECAXSA-N (Z)-7-Hexadecen-1,16-olide Chemical compound O=C1CCCCC\C=C/CCCCCCCCO1 NVIPUOMWGQAOIT-RQOWECAXSA-N 0.000 claims description 4
ZKVZSBSZTMPBQR-OWOJBTEDSA-N (Z)-9-Cycloheptadecen-1-one Chemical compound O=C1CCCCCCC\C=C\CCCCCCC1 ZKVZSBSZTMPBQR-OWOJBTEDSA-N 0.000 claims description 4
WSTQLNQRVZNEDV-CSKARUKUSA-N (e)-4-methyldec-3-en-5-ol Chemical compound CCCCCC(O)C(\C)=C\CC WSTQLNQRVZNEDV-CSKARUKUSA-N 0.000 claims description 4
HBBONAOKVLYWBI-KTKRTIGZSA-N (z)-dodec-3-enal Chemical compound CCCCCCCC\C=C/CC=O HBBONAOKVLYWBI-KTKRTIGZSA-N 0.000 claims description 4
ZCMKNGQFIXAHLP-UHFFFAOYSA-N 1,1,2,3,3-pentamethyl-2h-indene Chemical compound C1=CC=C2C(C)(C)C(C)C(C)(C)C2=C1 ZCMKNGQFIXAHLP-UHFFFAOYSA-N 0.000 claims description 4
RPJGIPAAHSGBEZ-UHFFFAOYSA-N 1,1-dimethoxynon-2-yne Chemical compound CCCCCCC#CC(OC)OC RPJGIPAAHSGBEZ-UHFFFAOYSA-N 0.000 claims description 4
QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical compound C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 claims description 4
MRMOPGVGWFNHIN-UHFFFAOYSA-N 1,6-dioxacycloheptadecan-7-one Chemical compound O=C1CCCCCCCCCCOCCCCO1 MRMOPGVGWFNHIN-UHFFFAOYSA-N 0.000 claims description 4
MZLRFHKWWCSGHB-UHFFFAOYSA-N 1,8-dioxacycloheptadecan-9-one Chemical compound O=C1CCCCCCCCOCCCCCCO1 MZLRFHKWWCSGHB-UHFFFAOYSA-N 0.000 claims description 4
VDBHOHJWUDKDRW-UHFFFAOYSA-N 1-(1,1,2,3,3,6-hexamethyl-2h-inden-5-yl)ethanone Chemical compound CC1=C(C(C)=O)C=C2C(C)(C)C(C)C(C)(C)C2=C1 VDBHOHJWUDKDRW-UHFFFAOYSA-N 0.000 claims description 4
XVULBTBTFGYVRC-UHFFFAOYSA-N 1-(3-hydroxy-3-methylpent-4-en-1-yl)-2,5,5,8a-tetramethyl-decahydronaphthalen-2-ol Chemical compound CC1(C)CCCC2(C)C(CCC(O)(C)C=C)C(C)(O)CCC21 XVULBTBTFGYVRC-UHFFFAOYSA-N 0.000 claims description 4
XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 claims description 4
ZNPGEERBEOWCEF-XVNBXDOJSA-N 1-cyclohexylethyl (e)-but-2-enoate Chemical compound C\C=C\C(=O)OC(C)C1CCCCC1 ZNPGEERBEOWCEF-XVNBXDOJSA-N 0.000 claims description 4
CNANHJLQJZEVPS-UHFFFAOYSA-N 1-ethoxyethoxycyclododecane Chemical compound CCOC(C)OC1CCCCCCCCCCC1 CNANHJLQJZEVPS-UHFFFAOYSA-N 0.000 claims description 4
PUQONFDEJWVBAS-UHFFFAOYSA-N 1-methyl-4-propan-2-yl-7-thiabicyclo[2.2.1]heptane Chemical compound C1CC2(C)CCC1(C(C)C)S2 PUQONFDEJWVBAS-UHFFFAOYSA-N 0.000 claims description 4
RTPMDRYHLHGFGT-UHFFFAOYSA-N 2',2',8',8'-tetramethylspiro[1,3-dioxolane-2,10'-octahydro-1h-2,4a-methanonapthalene] Chemical compound CC1(C)C(C2)CCC2(C(CC2)(C)C)C1C12OCCO1 RTPMDRYHLHGFGT-UHFFFAOYSA-N 0.000 claims description 4
OEBIUKPSCOVDQZ-UHFFFAOYSA-N 2,2,6,8-tetramethyl-3,4,4a,5,8,8a-hexahydro-1h-naphthalen-1-ol Chemical compound C1CC(C)(C)C(O)C2C(C)C=C(C)CC21 OEBIUKPSCOVDQZ-UHFFFAOYSA-N 0.000 claims description 4
IEZPIUQRQRWIFE-UHFFFAOYSA-N 2,4,6-trimethyl-4-phenyl-1,3-dioxane Chemical compound O1C(C)OC(C)CC1(C)C1=CC=CC=C1 IEZPIUQRQRWIFE-UHFFFAOYSA-N 0.000 claims description 4
UEGBWDUVDAKUGA-UHFFFAOYSA-N 2,6,10-trimethylundec-9-enal Chemical compound CC(C)=CCCC(C)CCCC(C)C=O UEGBWDUVDAKUGA-UHFFFAOYSA-N 0.000 claims description 4
MBZCATXQAHUZEZ-UHFFFAOYSA-N 2,6,10-trimethylundecanal Chemical compound CC(C)CCCC(C)CCCC(C)C=O MBZCATXQAHUZEZ-UHFFFAOYSA-N 0.000 claims description 4
CBOBADCVMLMQRW-UHFFFAOYSA-N 2,6-dimethyloctanal Chemical compound CCC(C)CCCC(C)C=O CBOBADCVMLMQRW-UHFFFAOYSA-N 0.000 claims description 4
DNRJTBAOUJJKDY-UHFFFAOYSA-N 2-Acetyl-3,5,5,6,8,8-hexamethyl-5,6,7,8- tetrahydronaphthalene Chemical compound CC(=O)C1=C(C)C=C2C(C)(C)C(C)CC(C)(C)C2=C1 DNRJTBAOUJJKDY-UHFFFAOYSA-N 0.000 claims description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 4
LUZDYPLAQQGJEA-UHFFFAOYSA-N 2-Methoxynaphthalene Chemical compound C1=CC=CC2=CC(OC)=CC=C21 LUZDYPLAQQGJEA-UHFFFAOYSA-N 0.000 claims description 4
SHSGYHAHMQLYRB-UHFFFAOYSA-N 2-Methyl-1-phenyl-2-propanyl butyrate Chemical compound CCCC(=O)OC(C)(C)CC1=CC=CC=C1 SHSGYHAHMQLYRB-UHFFFAOYSA-N 0.000 claims description 4
HMKKIXGYKWDQSV-SDNWHVSQSA-N 2-Pentyl-3-phenyl-2-propenal Chemical compound CCCCC\C(C=O)=C/C1=CC=CC=C1 HMKKIXGYKWDQSV-SDNWHVSQSA-N 0.000 claims description 4
ZNSALEJHPSBXDK-JLHYYAGUSA-N 2-[(2e)-3,7-dimethylocta-2,6-dienyl] cyclopentan-1-one Chemical compound CC(C)=CCC\C(C)=C\CC1CCCC1=O ZNSALEJHPSBXDK-JLHYYAGUSA-N 0.000 claims description 4
XSAYZAUNJMRRIR-UHFFFAOYSA-N 2-acetylnaphthalene Chemical compound C1=CC=CC2=CC(C(=O)C)=CC=C21 XSAYZAUNJMRRIR-UHFFFAOYSA-N 0.000 claims description 4
WKHTUDYDJUHYMK-UHFFFAOYSA-N 2-cyclododecylpropan-1-ol Chemical compound OCC(C)C1CCCCCCCCCCC1 WKHTUDYDJUHYMK-UHFFFAOYSA-N 0.000 claims description 4
PJXHBTZLHITWFX-UHFFFAOYSA-N 2-heptylcyclopentan-1-one Chemical compound CCCCCCCC1CCCC1=O PJXHBTZLHITWFX-UHFFFAOYSA-N 0.000 claims description 4
JTHVYOIHZNYRCC-UHFFFAOYSA-N 2-hexylcyclopentan-1-one Chemical compound CCCCCCC1CCCC1=O JTHVYOIHZNYRCC-UHFFFAOYSA-N 0.000 claims description 4
KVKKTLBBYFABAZ-UHFFFAOYSA-N 2-phenylethyl 2-methylbutanoate Chemical compound CCC(C)C(=O)OCCC1=CC=CC=C1 KVKKTLBBYFABAZ-UHFFFAOYSA-N 0.000 claims description 4
DLHQZZUEERVIGQ-UHFFFAOYSA-N 3,7-dimethyl-3-octanol Chemical compound CCC(C)(O)CCCC(C)C DLHQZZUEERVIGQ-UHFFFAOYSA-N 0.000 claims description 4
UCSIFMPORANABL-UHFFFAOYSA-N 3,7-dimethyloctanal Chemical compound CC(C)CCCC(C)CC=O UCSIFMPORANABL-UHFFFAOYSA-N 0.000 claims description 4
OHRBQTOZYGEWCJ-UHFFFAOYSA-N 3-(3-propan-2-ylphenyl)butanal Chemical compound CC(C)C1=CC=CC(C(C)CC=O)=C1 OHRBQTOZYGEWCJ-UHFFFAOYSA-N 0.000 claims description 4
AEJRTNBCFUOSEM-UHFFFAOYSA-N 3-Methyl-1-phenyl-3-pentanol Chemical compound CCC(C)(O)CCC1=CC=CC=C1 AEJRTNBCFUOSEM-UHFFFAOYSA-N 0.000 claims description 4
FKLSTTWRGDCXOK-UHFFFAOYSA-N 3-methoxy-7,7-dimethyl-10-methylidenebicyclo[4.3.1]decane Chemical compound C1C(OC)CCC2C(C)(C)CCC1C2=C FKLSTTWRGDCXOK-UHFFFAOYSA-N 0.000 claims description 4
ZISGOYMWXFOWAM-UHFFFAOYSA-N 3-methyl-2-pentylcyclopentan-1-one Chemical compound CCCCCC1C(C)CCC1=O ZISGOYMWXFOWAM-UHFFFAOYSA-N 0.000 claims description 4
FVKRIDSRWFEQME-UHFFFAOYSA-N 3-methylbutyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCC(C)C FVKRIDSRWFEQME-UHFFFAOYSA-N 0.000 claims description 4
INIOTLARNNSXAE-UHFFFAOYSA-N 4,8-dimethyl-2-propan-2-ylidene-3,3a,4,5,6,8a-hexahydro-1h-azulen-6-ol Chemical compound CC1CC(O)C=C(C)C2CC(=C(C)C)CC12 INIOTLARNNSXAE-UHFFFAOYSA-N 0.000 claims description 4
DCSKAMGZSIRJAQ-UHFFFAOYSA-N 4-(2-methylbutan-2-yl)cyclohexan-1-one Chemical compound CCC(C)(C)C1CCC(=O)CC1 DCSKAMGZSIRJAQ-UHFFFAOYSA-N 0.000 claims description 4
YZRXRLLRSPQHDK-UHFFFAOYSA-N 6-Hexyltetrahydro-2H-pyran-2-one Chemical compound CCCCCCC1CCCC(=O)O1 YZRXRLLRSPQHDK-UHFFFAOYSA-N 0.000 claims description 4
OSMLMQQJZVENMX-UHFFFAOYSA-N 6-butyl-2,4-dimethyl-3,6-dihydro-2h-pyran Chemical compound CCCCC1OC(C)CC(C)=C1 OSMLMQQJZVENMX-UHFFFAOYSA-N 0.000 claims description 4
QNEXACLQEWOALO-UHFFFAOYSA-N 67634-20-2 Chemical compound C12C=CCC2C2CC(OC(=O)C(C)C)C1C2 QNEXACLQEWOALO-UHFFFAOYSA-N 0.000 claims description 4
QGFSQVPRCWJZQK-UHFFFAOYSA-N 9-Decen-1-ol Chemical compound OCCCCCCCCC=C QGFSQVPRCWJZQK-UHFFFAOYSA-N 0.000 claims description 4
LGOFSGDSFQNIAT-SCRDCRAPSA-N Bulnesol Chemical compound C1C[C@@H](C(C)(C)O)C[C@H]2[C@@H](C)CCC2=C1C LGOFSGDSFQNIAT-SCRDCRAPSA-N 0.000 claims description 4
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 claims description 4
WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 claims description 4
DWZRENGNFQNWQZ-DHZHZOJOSA-N Citral propylene glycol acetal Chemical compound CC1COC(\C=C(/C)CCC=C(C)C)O1 DWZRENGNFQNWQZ-DHZHZOJOSA-N 0.000 claims description 4
HTIRHQRTDBPHNZ-UHFFFAOYSA-N Dibutyl sulfide Chemical compound CCCCSCCCC HTIRHQRTDBPHNZ-UHFFFAOYSA-N 0.000 claims description 4
AJUWUYJULVYGRA-UHFFFAOYSA-N Dodecanal dimethyl acetal Chemical compound CCCCCCCCCCCC(OC)OC AJUWUYJULVYGRA-UHFFFAOYSA-N 0.000 claims description 4
102000004190 Enzymes Human genes 0.000 claims description 4
108090000790 Enzymes Proteins 0.000 claims description 4
FXNFFCMITPHEIT-UHFFFAOYSA-N Ethyl 10-undecenoate Chemical compound CCOC(=O)CCCCCCCCC=C FXNFFCMITPHEIT-UHFFFAOYSA-N 0.000 claims description 4
XRHCAGNSDHCHFJ-UHFFFAOYSA-N Ethylene brassylate Chemical compound O=C1CCCCCCCCCCCC(=O)OCCO1 XRHCAGNSDHCHFJ-UHFFFAOYSA-N 0.000 claims description 4
TWVJWDMOZJXUID-SDDRHHMPSA-N Guaiol Chemical compound C1([C@H](CC[C@H](C2)C(C)(C)O)C)=C2[C@@H](C)CC1 TWVJWDMOZJXUID-SDDRHHMPSA-N 0.000 claims description 4
OOYRHNIVDZZGQV-UHFFFAOYSA-N Khusenol Chemical compound C=C1C(C)(C)C(C2)CCC32C(CO)CCC31 OOYRHNIVDZZGQV-UHFFFAOYSA-N 0.000 claims description 4
JZIARAQCPRDGAC-UHFFFAOYSA-N Linalyl isobutyrate Chemical compound CC(C)C(=O)OC(C)(C=C)CCC=C(C)C JZIARAQCPRDGAC-UHFFFAOYSA-N 0.000 claims description 4
ZWNPUELCBZVMDA-CMDGGOBGSA-N Methyl 2-nonenoate Chemical compound CCCCCC\C=C\C(=O)OC ZWNPUELCBZVMDA-CMDGGOBGSA-N 0.000 claims description 4
FRLZQXRXIKQFNS-UHFFFAOYSA-N Methyl 2-octynoate Chemical compound CCCCCC#CC(=O)OC FRLZQXRXIKQFNS-UHFFFAOYSA-N 0.000 claims description 4
SUAUILGSCPYJCS-UHFFFAOYSA-N Musk ambrette Chemical compound COC1=C([N+]([O-])=O)C(C)=C([N+]([O-])=O)C=C1C(C)(C)C SUAUILGSCPYJCS-UHFFFAOYSA-N 0.000 claims description 4
PTJICCHLTNPHDB-UHFFFAOYSA-N Octanal propyleneglycol acetal Chemical compound CCCCCCCC1OCC(C)O1 PTJICCHLTNPHDB-UHFFFAOYSA-N 0.000 claims description 4
WVTHGLPXSATJHZ-UHFFFAOYSA-N Octyl 2-furoate Chemical compound CCCCCCCCOC(=O)C1=CC=CO1 WVTHGLPXSATJHZ-UHFFFAOYSA-N 0.000 claims description 4
CRFQQFDSKWNZIZ-YYDJUVGSSA-N [(2e)-3,7-dimethylocta-2,6-dienyl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC\C=C(/C)CCC=C(C)C CRFQQFDSKWNZIZ-YYDJUVGSSA-N 0.000 claims description 4
KLKQSZIWHVEARN-RMKNXTFCSA-N [(e)-3-phenylprop-2-enyl] 2-methylpropanoate Chemical compound CC(C)C(=O)OC\C=C\C1=CC=CC=C1 KLKQSZIWHVEARN-RMKNXTFCSA-N 0.000 claims description 4
JMFFUDMJDZXYCT-BQYQJAHWSA-N [(e)-hept-1-enyl] acetate Chemical compound CCCCC\C=C\OC(C)=O JMFFUDMJDZXYCT-BQYQJAHWSA-N 0.000 claims description 4
IGODOXYLBBXFDW-UHFFFAOYSA-N alpha-Terpinyl acetate Chemical compound CC(=O)OC(C)(C)C1CCC(C)=CC1 IGODOXYLBBXFDW-UHFFFAOYSA-N 0.000 claims description 4
OJYKYCDSGQGTRJ-GQYWAMEOSA-N beta-santalol Chemical compound C1C[C@H]2C(=C)[C@@](CC/C=C(CO)/C)(C)[C@@H]1C2 OJYKYCDSGQGTRJ-GQYWAMEOSA-N 0.000 claims description 4
PHWISBHSBNDZDX-LSDHHAIUSA-N beta-sesquiphellandrene Chemical compound CC(C)=CCC[C@H](C)[C@H]1CCC(=C)C=C1 PHWISBHSBNDZDX-LSDHHAIUSA-N 0.000 claims description 4
FZJUFJKVIYFBSY-UHFFFAOYSA-N bourgeonal Chemical compound CC(C)(C)C1=CC=C(CCC=O)C=C1 FZJUFJKVIYFBSY-UHFFFAOYSA-N 0.000 claims description 4
JKKGTSUICJWEKB-SREVYHEPSA-N cis-3-Hexenyl 2-methylbutanoate Chemical compound CC\C=C/CCOC(=O)C(C)CC JKKGTSUICJWEKB-SREVYHEPSA-N 0.000 claims description 4
NUQDJSMHGCTKNL-UHFFFAOYSA-N cyclohexyl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1CCCCC1 NUQDJSMHGCTKNL-UHFFFAOYSA-N 0.000 claims description 4
KATXJJSCAPBIOB-UHFFFAOYSA-N cyclotetradecane Chemical compound C1CCCCCCCCCCCCC1 KATXJJSCAPBIOB-UHFFFAOYSA-N 0.000 claims description 4
AKMSQWLDTSOVME-UHFFFAOYSA-N dec-9-enal Chemical compound C=CCCCCCCCC=O AKMSQWLDTSOVME-UHFFFAOYSA-N 0.000 claims description 4
YHAJBLWYOIUHHM-GUTXKFCHSA-N delta-guaiene Chemical compound C1C[C@@H](C(C)=C)C[C@H]2[C@@H](C)CCC2=C1C YHAJBLWYOIUHHM-GUTXKFCHSA-N 0.000 claims description 4
MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 claims description 4
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims description 4
CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 claims description 4
GFJIQNADMLPFOW-VNHYZAJKSA-N elemol Chemical compound CC(=C)[C@@H]1C[C@H](C(C)(C)O)CC[C@@]1(C)C=C GFJIQNADMLPFOW-VNHYZAJKSA-N 0.000 claims description 4
VQNUNMBDOKEZHS-UHFFFAOYSA-N ethoxymethoxycyclododecane Chemical compound CCOCOC1CCCCCCCCCCC1 VQNUNMBDOKEZHS-UHFFFAOYSA-N 0.000 claims description 4
OPCRGEVPIBLWAY-OCBXPSTGSA-N ethyl (2z,4e)-deca-2,4-dienoate Chemical compound CCCCC\C=C\C=C/C(=O)OCC OPCRGEVPIBLWAY-OCBXPSTGSA-N 0.000 claims description 4
VZRGLBPRLIGTPE-UHFFFAOYSA-N furan-2-ylmethyl heptanoate Chemical compound CCCCCCC(=O)OCC1=CC=CO1 VZRGLBPRLIGTPE-UHFFFAOYSA-N 0.000 claims description 4
IQDXAJNQKSIPGB-HQSZAHFGSA-N geranyllinalool Chemical compound CC(C)=CCC\C(C)=C\CC\C(C)=C\CCC(C)(O)C=C IQDXAJNQKSIPGB-HQSZAHFGSA-N 0.000 claims description 4
UJPPXNXOEVDSRW-UHFFFAOYSA-N isopropyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC(C)C UJPPXNXOEVDSRW-UHFFFAOYSA-N 0.000 claims description 4
XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 claims description 4
239000004816 latex Substances 0.000 claims description 4
229920000126 latex Polymers 0.000 claims description 4
WDSOYUINLRIGNV-UHFFFAOYSA-N methoxycyclododecane Chemical compound COC1CCCCCCCCCCC1 WDSOYUINLRIGNV-UHFFFAOYSA-N 0.000 claims description 4
NTLJTUMJJWVCTL-UHFFFAOYSA-N methyl non-2-ynoate Chemical compound CCCCCCC#CC(=O)OC NTLJTUMJJWVCTL-UHFFFAOYSA-N 0.000 claims description 4
YSIMAPNUZAVQER-UHFFFAOYSA-N octanenitrile Chemical compound CCCCCCCC#N YSIMAPNUZAVQER-UHFFFAOYSA-N 0.000 claims description 4
DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 claims description 4
OJEQSSJFSNLMLB-UHFFFAOYSA-N p-Tolyl phenylacetate Chemical compound C1=CC(C)=CC=C1OC(=O)CC1=CC=CC=C1 OJEQSSJFSNLMLB-UHFFFAOYSA-N 0.000 claims description 4
RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 claims description 4
NDTYTMIUWGWIMO-UHFFFAOYSA-N perillyl alcohol Chemical compound CC(=C)C1CCC(CO)=CC1 NDTYTMIUWGWIMO-UHFFFAOYSA-N 0.000 claims description 4
FCJSHPDYVMKCHI-UHFFFAOYSA-N phenyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1 FCJSHPDYVMKCHI-UHFFFAOYSA-N 0.000 claims description 4
NDVASEGYNIMXJL-UHFFFAOYSA-N sabinene Chemical compound C=C1CCC2(C(C)C)C1C2 NDVASEGYNIMXJL-UHFFFAOYSA-N 0.000 claims description 4
MLRCLPRHEOPXLL-UHFFFAOYSA-N tetradecanenitrile Chemical compound CCCCCCCCCCCCCC#N MLRCLPRHEOPXLL-UHFFFAOYSA-N 0.000 claims description 4
KVQOADNSNSUAJT-UHFFFAOYSA-N α-patchoulene Chemical compound CC1=CCC(C2(C)C)CC3C12CCC3C KVQOADNSNSUAJT-UHFFFAOYSA-N 0.000 claims description 4
WTVHAMTYZJGJLJ-LSDHHAIUSA-N β-bisabolol Chemical compound CC(C)=CCC[C@H](C)[C@]1(O)CCC(C)=CC1 WTVHAMTYZJGJLJ-LSDHHAIUSA-N 0.000 claims description 4
YKFLAYDHMOASIY-UHFFFAOYSA-N γ-terpinene Chemical compound CC(C)C1=CCC(C)=CC1 YKFLAYDHMOASIY-UHFFFAOYSA-N 0.000 claims description 4
NEHNMFOYXAPHSD-SNVBAGLBSA-N (+)-Citronellal Chemical compound O=CC[C@H](C)CCC=C(C)C NEHNMFOYXAPHSD-SNVBAGLBSA-N 0.000 claims description 3
FUCYIEXQVQJBKY-ZFWWWQNUSA-N (+)-δ-Cadinene Chemical compound C1CC(C)=C[C@H]2[C@H](C(C)C)CCC(C)=C21 FUCYIEXQVQJBKY-ZFWWWQNUSA-N 0.000 claims description 3
LHYHMMRYTDARSZ-AJNGGQMLSA-N (-)-Tau-muurolol Chemical compound C1CC(C)=C[C@H]2[C@H](C(C)C)CC[C@](C)(O)[C@H]21 LHYHMMRYTDARSZ-AJNGGQMLSA-N 0.000 claims description 3
NFLGAXVYCFJBMK-BDAKNGLRSA-N (-)-menthone Chemical compound CC(C)[C@@H]1CC[C@@H](C)CC1=O NFLGAXVYCFJBMK-BDAKNGLRSA-N 0.000 claims description 3
VMYXUZSZMNBRCN-CQSZACIVSA-N (-)-α-curcumene Chemical compound CC(C)=CCC[C@@H](C)C1=CC=C(C)C=C1 VMYXUZSZMNBRCN-CQSZACIVSA-N 0.000 claims description 3
XMGQYMWWDOXHJM-SNVBAGLBSA-N (-)-α-limonene Chemical compound CC(=C)[C@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-SNVBAGLBSA-N 0.000 claims description 3
HZRFVTRTTXBHSE-RIMRTXSHSA-N (1R,2R,5S,7R,8R,10S)-2,6,6,8-tetramethyl-9-oxatetracyclo[5.4.1.01,5.08,10]dodecane Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1[C@@]1(C)O[C@H]1C2 HZRFVTRTTXBHSE-RIMRTXSHSA-N 0.000 claims description 3
PUWNTRHCKNHSAT-KBPBESRZSA-N (1R,6S)-γ-himachalene Chemical compound CC1=CCCC(C)(C)[C@@H]2[C@H]1CCC(C)=C2 PUWNTRHCKNHSAT-KBPBESRZSA-N 0.000 claims description 3
FAMPSKZZVDUYOS-PGPZXUPKSA-N (1Z,4E,8Z)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene Chemical compound C\C1=C\CC(C)(C)\C=C\C\C(C)=C/CC1 FAMPSKZZVDUYOS-PGPZXUPKSA-N 0.000 claims description 3
WRHGORWNJGOVQY-QLFBSQMISA-N (1r,4ar,8as)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1h-naphthalene Chemical compound C1CC(C)=C[C@@H]2[C@@H](C(C)C)CCC(=C)[C@@H]21 WRHGORWNJGOVQY-QLFBSQMISA-N 0.000 claims description 3
XOKSLPVRUOBDEW-DJLDLDEBSA-N (1r,4s,5r)-4,6,6-trimethylbicyclo[3.1.1]heptane Chemical compound C[C@H]1CC[C@H]2C(C)(C)[C@@H]1C2 XOKSLPVRUOBDEW-DJLDLDEBSA-N 0.000 claims description 3
FUCYIEXQVQJBKY-DZGCQCFKSA-N (1s,8as)-4,7-dimethyl-1-propan-2-yl-1,2,3,5,6,8a-hexahydronaphthalene Chemical compound C1CC(C)=C[C@@H]2[C@H](C(C)C)CCC(C)=C21 FUCYIEXQVQJBKY-DZGCQCFKSA-N 0.000 claims description 3
KOSQMCNVEGXSCQ-UHFFFAOYSA-N (2-butan-2-yl-1-ethenylcyclohexyl) acetate Chemical compound CCC(C)C1CCCCC1(OC(C)=O)C=C KOSQMCNVEGXSCQ-UHFFFAOYSA-N 0.000 claims description 3
DCXXKSXLKWAZNO-UHFFFAOYSA-N (2-methyl-6-methylideneoct-7-en-2-yl) acetate Chemical compound CC(=O)OC(C)(C)CCCC(=C)C=C DCXXKSXLKWAZNO-UHFFFAOYSA-N 0.000 claims description 3
ZSKAJFSSXURRGL-PKNBQFBNSA-N (2e)-1,1-dimethoxy-3,7-dimethylocta-2,6-diene Chemical compound COC(OC)\C=C(/C)CCC=C(C)C ZSKAJFSSXURRGL-PKNBQFBNSA-N 0.000 claims description 3
HLCSDJLATUNSSI-JXMROGBWSA-N (2e)-3,7-dimethylocta-2,6-dienenitrile Chemical compound CC(C)=CCC\C(C)=C\C#N HLCSDJLATUNSSI-JXMROGBWSA-N 0.000 claims description 3
BCOXBEHFBZOJJZ-ARJAWSKDSA-N (3Z)-hex-3-en-1-yl benzoate Chemical compound CC\C=C/CCOC(=O)C1=CC=CC=C1 BCOXBEHFBZOJJZ-ARJAWSKDSA-N 0.000 claims description 3
DBWSGRFEGVADLQ-ZHACJKMWSA-N (3e)-trideca-3,12-dienenitrile Chemical compound C=CCCCCCCC\C=C\CC#N DBWSGRFEGVADLQ-ZHACJKMWSA-N 0.000 claims description 3
CUKVJQWRXQTFRF-UHFFFAOYSA-N (4-methylphenyl) hexanoate Chemical compound CCCCCC(=O)OC1=CC=C(C)C=C1 CUKVJQWRXQTFRF-UHFFFAOYSA-N 0.000 claims description 3
WTXBCFKGCNWPLS-UHFFFAOYSA-N (4-prop-1-en-2-yl-1-cyclohexenyl)methyl acetate Chemical compound CC(=O)OCC1=CCC(C(C)=C)CC1 WTXBCFKGCNWPLS-UHFFFAOYSA-N 0.000 claims description 3
WNRBYZQFEBIUGD-LSDHHAIUSA-N (4ar,8ar)-5,8a-dimethyl-3-propan-2-ylidene-1,2,4,4a,7,8-hexahydronaphthalene Chemical compound C1CC=C(C)[C@@H]2CC(=C(C)C)CC[C@]21C WNRBYZQFEBIUGD-LSDHHAIUSA-N 0.000 claims description 3
PHXATPHONSXBIL-SNVBAGLBSA-N (5r)-5-heptyloxolan-2-one Chemical compound CCCCCCC[C@@H]1CCC(=O)O1 PHXATPHONSXBIL-SNVBAGLBSA-N 0.000 claims description 3
FQTLCLSUCSAZDY-SDNWHVSQSA-N (6E)-nerolidol Chemical compound CC(C)=CCC\C(C)=C\CCC(C)(O)C=C FQTLCLSUCSAZDY-SDNWHVSQSA-N 0.000 claims description 3
239000001149 (9Z,12Z)-octadeca-9,12-dienoate Substances 0.000 claims description 3
KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 claims description 3
FQMZVFJYMPNUCT-YRNVUSSQSA-N (E)-geranyl formate Chemical compound CC(C)=CCC\C(C)=C\COC=O FQMZVFJYMPNUCT-YRNVUSSQSA-N 0.000 claims description 3
BSAIUMLZVGUGKX-BQYQJAHWSA-N (E)-non-2-enal Chemical compound CCCCCC\C=C\C=O BSAIUMLZVGUGKX-BQYQJAHWSA-N 0.000 claims description 3
LCOSCMLXPAQCLQ-AWEZNQCLSA-N (R)-β-himachalene Chemical compound C1CC(C)=C[C@H]2C1=C(C)CCCC2(C)C LCOSCMLXPAQCLQ-AWEZNQCLSA-N 0.000 claims description 3
VLUMOWNVWOXZAU-VQHVLOKHSA-N (e)-2-methyl-3-phenylprop-2-enal Chemical compound O=CC(/C)=C/C1=CC=CC=C1 VLUMOWNVWOXZAU-VQHVLOKHSA-N 0.000 claims description 3
FJCQUJKUMKZEMH-YRNVUSSQSA-N (e)-2-methyl-4-(2,6,6-trimethylcyclohexen-1-yl)but-2-enal Chemical compound O=CC(/C)=C/CC1=C(C)CCCC1(C)C FJCQUJKUMKZEMH-YRNVUSSQSA-N 0.000 claims description 3
YQUFLLFXOARBNW-PKNBQFBNSA-N (e)-4-(2,2-dimethyl-6-methylidenecyclohexyl)-3-methylbut-3-en-2-one Chemical compound CC(=O)C(\C)=C\C1C(=C)CCCC1(C)C YQUFLLFXOARBNW-PKNBQFBNSA-N 0.000 claims description 3
HAPNXLWNFLTTIE-JLHYYAGUSA-N (e)-8-indol-1-yl-2,6-dimethyloct-7-en-2-ol Chemical compound C1=CC=C2N(/C=C/C(CCCC(C)(C)O)C)C=CC2=C1 HAPNXLWNFLTTIE-JLHYYAGUSA-N 0.000 claims description 3
WOVJAWMZNOWDII-BQYQJAHWSA-N (e)-non-2-enenitrile Chemical compound CCCCCC\C=C\C#N WOVJAWMZNOWDII-BQYQJAHWSA-N 0.000 claims description 3
JRJBVWJSTHECJK-LUAWRHEFSA-N (z)-3-methyl-4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one Chemical compound CC(=O)C(\C)=C/C1C(C)=CCCC1(C)C JRJBVWJSTHECJK-LUAWRHEFSA-N 0.000 claims description 3
WKSPQBFDRTUGEF-QXMHVHEDSA-N (z)-tridec-2-enenitrile Chemical compound CCCCCCCCCC\C=C/C#N WKSPQBFDRTUGEF-QXMHVHEDSA-N 0.000 claims description 3
NTXGFKWLJFHGGJ-ACCUITESSA-N 1,1-Diethoxy-3,7-dimethyl-2,6-octadiene Chemical compound CCOC(OCC)\C=C(/C)CCC=C(C)C NTXGFKWLJFHGGJ-ACCUITESSA-N 0.000 claims description 3
BZOOCKAFKVYAOZ-UHFFFAOYSA-N 1,1-Dimethoxyoctane Chemical compound CCCCCCCC(OC)OC BZOOCKAFKVYAOZ-UHFFFAOYSA-N 0.000 claims description 3
GDDPLWAEEWIQKZ-UHFFFAOYSA-N 1,1-diethoxydecane Chemical compound CCCCCCCCCC(OCC)OCC GDDPLWAEEWIQKZ-UHFFFAOYSA-N 0.000 claims description 3
QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 claims description 3
RHKPJTFLRQNNGJ-UHFFFAOYSA-N 1,3-benzothiazole-2-carbaldehyde Chemical compound C1=CC=C2SC(C=O)=NC2=C1 RHKPJTFLRQNNGJ-UHFFFAOYSA-N 0.000 claims description 3
MKEIDVFLAWJKMY-UHFFFAOYSA-N 1,7-dioxacycloheptadecan-8-one Chemical compound O=C1CCCCCCCCCOCCCCCO1 MKEIDVFLAWJKMY-UHFFFAOYSA-N 0.000 claims description 3
GQBVHGLNSHPKPG-UHFFFAOYSA-N 1-(2-tert-butylcyclohexyl)oxybutan-2-ol Chemical compound CCC(O)COC1CCCCC1C(C)(C)C GQBVHGLNSHPKPG-UHFFFAOYSA-N 0.000 claims description 3
OHYNEUHOSWPWLZ-UHFFFAOYSA-N 1-(3,3-dimethylcyclohexyl)pent-4-en-1-one Chemical compound CC1(C)CCCC(C(=O)CCC=C)C1 OHYNEUHOSWPWLZ-UHFFFAOYSA-N 0.000 claims description 3
OEVIJAZJVZDBQL-UHFFFAOYSA-N 1-(5,5-dimethylcyclohexen-1-yl)pent-4-en-1-one Chemical compound CC1(C)CCC=C(C(=O)CCC=C)C1 OEVIJAZJVZDBQL-UHFFFAOYSA-N 0.000 claims description 3
KBHWKXNXTURZCD-UHFFFAOYSA-N 1-Methoxy-4-propylbenzene Chemical compound CCCC1=CC=C(OC)C=C1 KBHWKXNXTURZCD-UHFFFAOYSA-N 0.000 claims description 3
WPFFGMCNILGTEA-UHFFFAOYSA-N 1-spiro[4.5]dec-8-en-9-ylpent-4-en-1-one Chemical compound C1C(C(=O)CCC=C)=CCCC11CCCC1 WPFFGMCNILGTEA-UHFFFAOYSA-N 0.000 claims description 3
GIEMHYCMBGELGY-UHFFFAOYSA-N 10-undecen-1-ol Chemical compound OCCCCCCCCCC=C GIEMHYCMBGELGY-UHFFFAOYSA-N 0.000 claims description 3
NUSRNVWNTPMBJA-UHFFFAOYSA-N 13-methyl-1-oxacyclopentadec-10-en-2-one Chemical compound CC1CCOC(=O)CCCCCCCC=CC1 NUSRNVWNTPMBJA-UHFFFAOYSA-N 0.000 claims description 3
HUYXPANWJVOYCI-UHFFFAOYSA-N 2,2,6,6,7,8,8-heptamethyl-3,3a,4,5,5a,7,8a,8b-octahydrocyclopenta[g][1]benzofuran Chemical compound CC1C(C)(C)C2CCC3CC(C)(C)OC3C2C1(C)C HUYXPANWJVOYCI-UHFFFAOYSA-N 0.000 claims description 3
QFQQCCDAGARSEN-UHFFFAOYSA-N 2,2,6,6,7,8,8-heptamethyl-4,5,7,8b-tetrahydro-3ah-cyclopenta[g][1,3]benzodioxole Chemical compound CC1(C)C(C)C(C)(C)C2=C1C1OC(C)(C)OC1CC2 QFQQCCDAGARSEN-UHFFFAOYSA-N 0.000 claims description 3
FYMOBFDUZIDKMI-UHFFFAOYSA-N 2,2-dimethyl-3-(3-methylphenyl)propan-1-ol Chemical compound CC1=CC=CC(CC(C)(C)CO)=C1 FYMOBFDUZIDKMI-UHFFFAOYSA-N 0.000 claims description 3
JEPWTUCYPWOCQV-UHFFFAOYSA-N 2,4-dimethyl-2-(5,5,8,8-tetramethyl-6,7-dihydronaphthalen-2-yl)-1,3-dioxolane Chemical compound O1C(C)COC1(C)C1=CC=C2C(C)(C)CCC(C)(C)C2=C1 JEPWTUCYPWOCQV-UHFFFAOYSA-N 0.000 claims description 3
KJAJQPSBQHSPCZ-UHFFFAOYSA-N 2,4-dimethyl-6-phenyl-3,6-dihydro-2h-pyran Chemical compound O1C(C)CC(C)=CC1C1=CC=CC=C1 KJAJQPSBQHSPCZ-UHFFFAOYSA-N 0.000 claims description 3
YFHKETGXYQOMGB-UHFFFAOYSA-N 2,6,6,7,8,8-hexamethyl-3,3a,4,5,5a,7,8a,8b-octahydro-2h-cyclopenta[g][1]benzofuran Chemical compound C1CC2C(C)(C)C(C)C(C)(C)C2C2OC(C)CC21 YFHKETGXYQOMGB-UHFFFAOYSA-N 0.000 claims description 3
FAQVGPWFQGGIPP-UHFFFAOYSA-N 2-(2-methylpropyl)quinoline Chemical compound C1=CC=CC2=NC(CC(C)C)=CC=C21 FAQVGPWFQGGIPP-UHFFFAOYSA-N 0.000 claims description 3
JJJPNTQYUJPWGQ-UHFFFAOYSA-N 2-(3-Phenylpropyl)pyridine Chemical compound C=1C=CC=NC=1CCCC1=CC=CC=C1 JJJPNTQYUJPWGQ-UHFFFAOYSA-N 0.000 claims description 3
VQKSHQQZPYHYOS-UHFFFAOYSA-N 2-(4-propan-2-ylcyclohexa-1,4-dien-1-yl)ethyl formate Chemical compound CC(C)C1=CCC(CCOC=O)=CC1 VQKSHQQZPYHYOS-UHFFFAOYSA-N 0.000 claims description 3
LIPHCKNQPJXUQF-SDNWHVSQSA-N 2-Benzylidene-1-heptanol Chemical compound CCCCC\C(CO)=C/C1=CC=CC=C1 LIPHCKNQPJXUQF-SDNWHVSQSA-N 0.000 claims description 3
HLMIVULQFMULRM-UHFFFAOYSA-N 2-cyclohexyloxyethylbenzene Chemical compound C1CCCCC1OCCC1=CC=CC=C1 HLMIVULQFMULRM-UHFFFAOYSA-N 0.000 claims description 3
VBQKNJGYWOBPMY-UHFFFAOYSA-N 2-heptyloxolane Chemical compound CCCCCCCC1CCCO1 VBQKNJGYWOBPMY-UHFFFAOYSA-N 0.000 claims description 3
VGECIEOJXLMWGO-UHFFFAOYSA-N 2-hexylcyclopent-2-en-1-one Chemical compound CCCCCCC1=CCCC1=O VGECIEOJXLMWGO-UHFFFAOYSA-N 0.000 claims description 3
239000001725 2-hexylcyclopent-2-en-1-one Substances 0.000 claims description 3
FPKBRMRMNGYJLA-UHFFFAOYSA-M 2-hydroxyethyl-methyl-bis(2-octadecanoyloxyethyl)azanium;methyl sulfate Chemical compound COS([O-])(=O)=O.CCCCCCCCCCCCCCCCCC(=O)OCC[N+](C)(CCO)CCOC(=O)CCCCCCCCCCCCCCCCC FPKBRMRMNGYJLA-UHFFFAOYSA-M 0.000 claims description 3
XPCSGXMQGQGBKU-UHFFFAOYSA-N 2-methyldecanenitrile Chemical compound CCCCCCCCC(C)C#N XPCSGXMQGQGBKU-UHFFFAOYSA-N 0.000 claims description 3
MWYGSCHWFNRSET-UHFFFAOYSA-N 2-pentylcyclopentan-1-ol Chemical compound CCCCCC1CCCC1O MWYGSCHWFNRSET-UHFFFAOYSA-N 0.000 claims description 3
ILZXXGLGJZQLTR-UHFFFAOYSA-N 2-phenylethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC1=CC=CC=C1 ILZXXGLGJZQLTR-UHFFFAOYSA-N 0.000 claims description 3
FMPXLXBVYDFXIC-UHFFFAOYSA-N 2-propan-2-yloxyethylbenzene Chemical compound CC(C)OCCC1=CC=CC=C1 FMPXLXBVYDFXIC-UHFFFAOYSA-N 0.000 claims description 3
NJABNUVNVZSEGN-UHFFFAOYSA-N 2-propylheptanenitrile Chemical compound CCCCCC(C#N)CCC NJABNUVNVZSEGN-UHFFFAOYSA-N 0.000 claims description 3
VMUNAKQXJLHODT-VAWYXSNFSA-N 2-tridecenal Chemical compound CCCCCCCCCC\C=C\C=O VMUNAKQXJLHODT-VAWYXSNFSA-N 0.000 claims description 3
JFKHPWLOPZASHC-UHFFFAOYSA-N 3,6-dimethyloctan-3-yl acetate Chemical compound CCC(C)CCC(C)(CC)OC(C)=O JFKHPWLOPZASHC-UHFFFAOYSA-N 0.000 claims description 3
ZGIGZINMAOQWLX-NCZFFCEISA-N 3,7,11-Trimethyl-2,6,10-dodecatrienyl acetate Chemical compound CC(C)=CCC\C(C)=C\CC\C(C)=C\COC(C)=O ZGIGZINMAOQWLX-NCZFFCEISA-N 0.000 claims description 3
MTDAKBBUYMYKAR-UHFFFAOYSA-N 3,7-dimethyloct-6-enenitrile Chemical compound N#CCC(C)CCC=C(C)C MTDAKBBUYMYKAR-UHFFFAOYSA-N 0.000 claims description 3
CVJBFMVLVJZZMM-UHFFFAOYSA-N 3,7-dimethyloct-6-enyl 2-phenylacetate Chemical compound CC(C)=CCCC(C)CCOC(=O)CC1=CC=CC=C1 CVJBFMVLVJZZMM-UHFFFAOYSA-N 0.000 claims description 3
UDPCCAUIDDVTEL-UHFFFAOYSA-N 3,7-dimethyloct-6-enyl benzoate Chemical compound CC(C)=CCCC(C)CCOC(=O)C1=CC=CC=C1 UDPCCAUIDDVTEL-UHFFFAOYSA-N 0.000 claims description 3
IVIORUOCIAMOLJ-UHFFFAOYSA-N 3-(4-methylcyclohex-3-en-1-yl)but-3-enyl acetate Chemical compound CC(=O)OCCC(=C)C1CCC(C)=CC1 IVIORUOCIAMOLJ-UHFFFAOYSA-N 0.000 claims description 3
JTVKFAPEIBMMHX-UHFFFAOYSA-N 3-(4-methylcyclohex-3-en-1-yl)butan-1-ol Chemical compound OCCC(C)C1CCC(C)=CC1 JTVKFAPEIBMMHX-UHFFFAOYSA-N 0.000 claims description 3
UIHGITHJVWASPE-UHFFFAOYSA-N 3-methyl-5-phenylpentanenitrile Chemical compound N#CCC(C)CCC1=CC=CC=C1 UIHGITHJVWASPE-UHFFFAOYSA-N 0.000 claims description 3
YAPZGQNSTVDGJX-BQYQJAHWSA-N 3-methylbutyl (e)-undec-6-enoate Chemical compound CCCC\C=C\CCCCC(=O)OCCC(C)C YAPZGQNSTVDGJX-BQYQJAHWSA-N 0.000 claims description 3
UZWOWEPOVKVMEL-UHFFFAOYSA-N 4-(2,2,6-trimethylcyclohexyl)butan-2-ol Chemical compound CC(O)CCC1C(C)CCCC1(C)C UZWOWEPOVKVMEL-UHFFFAOYSA-N 0.000 claims description 3
MQBIZQLCHSZBOI-UHFFFAOYSA-N 4-(4-Methyl-3-pentenyl)-3-cyclohexene-1-carboxaldehyde Chemical compound CC(C)=CCCC1=CCC(C=O)CC1 MQBIZQLCHSZBOI-UHFFFAOYSA-N 0.000 claims description 3
CWRKZMLUDFBPAO-SREVYHEPSA-N 4-Decenal Chemical compound CCCCC\C=C/CCC=O CWRKZMLUDFBPAO-SREVYHEPSA-N 0.000 claims description 3
OSDLLIBGSJNGJE-UHFFFAOYSA-N 4-chloro-3,5-dimethylphenol Chemical compound CC1=CC(O)=CC(C)=C1Cl OSDLLIBGSJNGJE-UHFFFAOYSA-N 0.000 claims description 3
ALWUKGXLBSQSMA-UHFFFAOYSA-N 5-Hexyldihydro-5-methyl-2(3H)-furanone Chemical compound CCCCCCC1(C)CCC(=O)O1 ALWUKGXLBSQSMA-UHFFFAOYSA-N 0.000 claims description 3
OWFZJSXGDOTWSH-UHFFFAOYSA-N 5-methyl-2-propan-2-ylbicyclo[2.2.2]oct-5-ene-8-carbaldehyde Chemical compound O=CC1CC2C(C(C)C)CC1C(C)=C2 OWFZJSXGDOTWSH-UHFFFAOYSA-N 0.000 claims description 3
RDHNTAXPFZIMDN-UHFFFAOYSA-N 6,6-Dimethoxy-2,5,5-trimethyl-2-hexene Chemical compound COC(OC)C(C)(C)CC=C(C)C RDHNTAXPFZIMDN-UHFFFAOYSA-N 0.000 claims description 3
AUBLFWWZTFFBNU-UHFFFAOYSA-N 6-butan-2-ylquinoline Chemical compound N1=CC=CC2=CC(C(C)CC)=CC=C21 AUBLFWWZTFFBNU-UHFFFAOYSA-N 0.000 claims description 3
UBALJTRHSDXCPY-WAPJZHGLSA-N 6-ethylideneoctahydro-5,8-methano-2h-benzo-1-pyran Chemical compound C12CCCOC2C2C/C(=C/C)C1C2 UBALJTRHSDXCPY-WAPJZHGLSA-N 0.000 claims description 3
QMXBURPYNWBMJR-UHFFFAOYSA-N 6-methoxy-2,6-dimethylheptanal Chemical compound COC(C)(C)CCCC(C)C=O QMXBURPYNWBMJR-UHFFFAOYSA-N 0.000 claims description 3
NKCQEIXYLHACJC-UHFFFAOYSA-N 6-propan-2-ylquinoline Chemical compound N1=CC=CC2=CC(C(C)C)=CC=C21 NKCQEIXYLHACJC-UHFFFAOYSA-N 0.000 claims description 3
KMRMUZKLFIEVAO-UHFFFAOYSA-N 7,7-dimethylbicyclo[3.1.1]hept-3-ene-4-carbaldehyde Chemical compound C1C2C(C)(C)C1CC=C2C=O KMRMUZKLFIEVAO-UHFFFAOYSA-N 0.000 claims description 3
OZQAPQSEYFAMCY-SOUVJXGZSA-N 7betaH-eudesma-3,11-diene Chemical compound C1CC=C(C)[C@@H]2C[C@@H](C(=C)C)CC[C@]21C OZQAPQSEYFAMCY-SOUVJXGZSA-N 0.000 claims description 3
YKLKFIPZNHLBMW-UHFFFAOYSA-N 8,8-di(indol-1-yl)-2,6-dimethyloctan-2-ol Chemical compound C1=CC2=CC=CC=C2N1C(CC(CCCC(C)(C)O)C)N1C2=CC=CC=C2C=C1 YKLKFIPZNHLBMW-UHFFFAOYSA-N 0.000 claims description 3
XZZRGHSODLRWGO-UHFFFAOYSA-N 9,11-dimethylspiro[5.5]undecan-3-one Chemical compound CC1CC(C)CCC11CCC(=O)CC1 XZZRGHSODLRWGO-UHFFFAOYSA-N 0.000 claims description 3
ZFMUIJVOIVHGCF-NSCUHMNNSA-N 9-undecenal Chemical compound C\C=C\CCCCCCCC=O ZFMUIJVOIVHGCF-NSCUHMNNSA-N 0.000 claims description 3
GRAORJFMGCQWRN-UHFFFAOYSA-N Butyl undecylenate Chemical compound CCCCOC(=O)CCCCCCCCC=C GRAORJFMGCQWRN-UHFFFAOYSA-N 0.000 claims description 3
KKVZAVRSVHUSPL-GQCTYLIASA-N Cassiastearoptene Chemical compound COC1=CC=CC=C1\C=C\C=O KKVZAVRSVHUSPL-GQCTYLIASA-N 0.000 claims description 3
NQBWNECTZUOWID-MZXMXVKLSA-N Cinnamyl cinnamate Chemical compound C=1C=CC=CC=1/C=C/C(=O)OC\C=C\C1=CC=CC=C1 NQBWNECTZUOWID-MZXMXVKLSA-N 0.000 claims description 3
NOTFZGFABLVTIG-UHFFFAOYSA-N Cyclohexylethyl acetate Chemical compound CC(=O)OCCC1CCCCC1 NOTFZGFABLVTIG-UHFFFAOYSA-N 0.000 claims description 3
VUNOFAIHSALQQH-UHFFFAOYSA-N Ethyl menthane carboxamide Chemical compound CCNC(=O)C1CC(C)CCC1C(C)C VUNOFAIHSALQQH-UHFFFAOYSA-N 0.000 claims description 3
JUWUWIGZUVEFQB-UHFFFAOYSA-N Fenchyl acetate Chemical compound C1CC2C(C)(C)C(OC(=O)C)C1(C)C2 JUWUWIGZUVEFQB-UHFFFAOYSA-N 0.000 claims description 3
JNIWCVWKECYDSV-UHFFFAOYSA-N Furfuryl octanoate Chemical compound CCCCCCCC(=O)OCC1=CC=CO1 JNIWCVWKECYDSV-UHFFFAOYSA-N 0.000 claims description 3
GAIBLDCXCZKKJE-YZJXYJLZSA-N Germacren D Chemical compound CC(C)C/1CC\C(C)=C\CCC(=C)\C=C\1 GAIBLDCXCZKKJE-YZJXYJLZSA-N 0.000 claims description 3
KMLFVAGUWNPADU-UHFFFAOYSA-N Hexyl 2-furoate Chemical compound CCCCCCOC(=O)C1=CC=CO1 KMLFVAGUWNPADU-UHFFFAOYSA-N 0.000 claims description 3
DUKPKQFHJQGTGU-UHFFFAOYSA-N Hexyl salicylic acid Chemical compound CCCCCCOC(=O)C1=CC=CC=C1O DUKPKQFHJQGTGU-UHFFFAOYSA-N 0.000 claims description 3
AXISYYRBXTVTFY-UHFFFAOYSA-N Isopropyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OC(C)C AXISYYRBXTVTFY-UHFFFAOYSA-N 0.000 claims description 3
WHIJSULEEDNKPD-UHFFFAOYSA-N Linalyl anthranilate Chemical compound CC(C)=CCCC(C)(C=C)OC(=O)C1=CC=CC=C1N WHIJSULEEDNKPD-UHFFFAOYSA-N 0.000 claims description 3
GECFTYLLVUKXOY-UHFFFAOYSA-N Menthone 1,3-glyceryl ketal Chemical compound CC(C)C1CCC(C)CC11OCC(O)CO1 GECFTYLLVUKXOY-UHFFFAOYSA-N 0.000 claims description 3
ALHUZKCOMYUFRB-OAHLLOKOSA-N Muscone Chemical compound C[C@@H]1CCCCCCCCCCCCC(=O)C1 ALHUZKCOMYUFRB-OAHLLOKOSA-N 0.000 claims description 3
MIYFJEKZLFWKLZ-UHFFFAOYSA-N Phenylmethyl benzeneacetate Chemical compound C=1C=CC=CC=1COC(=O)CC1=CC=CC=C1 MIYFJEKZLFWKLZ-UHFFFAOYSA-N 0.000 claims description 3
BCOXBEHFBZOJJZ-UHFFFAOYSA-N Z-hex-3-en-1-yl benzoate Natural products CCC=CCCOC(=O)C1=CC=CC=C1 BCOXBEHFBZOJJZ-UHFFFAOYSA-N 0.000 claims description 3
CMJSVJIGLBDCME-FOWTUZBSSA-N [(2e)-2-benzylideneheptyl] acetate Chemical compound CCCCC\C(COC(C)=O)=C/C1=CC=CC=C1 CMJSVJIGLBDCME-FOWTUZBSSA-N 0.000 claims description 3
KGDJMNKPBUNHGY-RMKNXTFCSA-N [(e)-3-phenylprop-2-enyl] propanoate Chemical compound CCC(=O)OC\C=C\C1=CC=CC=C1 KGDJMNKPBUNHGY-RMKNXTFCSA-N 0.000 claims description 3
OAKFACUIGQLOCA-UHFFFAOYSA-N [1-methyl-2-[(1,2,2-trimethyl-3-bicyclo[3.1.0]hexanyl)methyl]cyclopropyl]methanol Chemical compound OCC1(C)CC1CC1C(C)(C)C2(C)CC2C1 OAKFACUIGQLOCA-UHFFFAOYSA-N 0.000 claims description 3
HTQLNWONIAXQKC-UHFFFAOYSA-N [4-(4-methylpent-3-enyl)cyclohex-3-en-1-yl]methyl acetate Chemical compound CC(C)=CCCC1=CCC(COC(C)=O)CC1 HTQLNWONIAXQKC-UHFFFAOYSA-N 0.000 claims description 3
LHYHMMRYTDARSZ-BYNSBNAKSA-N alpha-cadinol Chemical compound C1CC(C)=C[C@H]2[C@H](C(C)C)CC[C@@](C)(O)[C@@H]21 LHYHMMRYTDARSZ-BYNSBNAKSA-N 0.000 claims description 3
GUUHFMWKWLOQMM-NTCAYCPXSA-N alpha-hexylcinnamaldehyde Chemical compound CCCCCC\C(C=O)=C/C1=CC=CC=C1 GUUHFMWKWLOQMM-NTCAYCPXSA-N 0.000 claims description 3
QMAYBMKBYCGXDH-ZNMIVQPWSA-N alpha-muurolene Chemical compound C1CC(C)=C[C@H]2[C@H](C(C)C)CC=C(C)[C@H]21 QMAYBMKBYCGXDH-ZNMIVQPWSA-N 0.000 claims description 3
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 3
239000001518 benzyl (E)-3-phenylprop-2-enoate Substances 0.000 claims description 3
229960002903 benzyl benzoate Drugs 0.000 claims description 3
QNRYOQRUGRVBRL-UHFFFAOYSA-N benzyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC1=CC=CC=C1 QNRYOQRUGRVBRL-UHFFFAOYSA-N 0.000 claims description 3
229930006722 beta-pinene Natural products 0.000 claims description 3
XAPCMTMQBXLDBB-UHFFFAOYSA-N butanoic acid hexyl ester Natural products CCCCCCOC(=O)CCC XAPCMTMQBXLDBB-UHFFFAOYSA-N 0.000 claims description 3
235000010354 butylated hydroxytoluene Nutrition 0.000 claims description 3
229930006739 camphene Natural products 0.000 claims description 3
RECUKUPTGUEGMW-UHFFFAOYSA-N carvacrol Chemical compound CC(C)C1=CC=C(C)C(O)=C1 RECUKUPTGUEGMW-UHFFFAOYSA-N 0.000 claims description 3
230000003197 catalytic effect Effects 0.000 claims description 3
IEPWIPZLLIOZLU-ARJAWSKDSA-N cis-3-Hexenyl salicylate Chemical compound CC\C=C/CCOC(=O)C1=CC=CC=C1O IEPWIPZLLIOZLU-ARJAWSKDSA-N 0.000 claims description 3
NNWHUJCUHAELCL-UHFFFAOYSA-N cis-Methyl isoeugenol Natural products COC1=CC=C(C=CC)C=C1OC NNWHUJCUHAELCL-UHFFFAOYSA-N 0.000 claims description 3
NGHOLYJTSCBCGC-UHFFFAOYSA-N cis-cinnamic acid benzyl ester Natural products C=1C=CC=CC=1C=CC(=O)OCC1=CC=CC=C1 NGHOLYJTSCBCGC-UHFFFAOYSA-N 0.000 claims description 3
235000000484 citronellol Nutrition 0.000 claims description 3
BLBJUGKATXCWET-UHFFFAOYSA-N cyclaprop Chemical compound C12CC=CC2C2CC(OC(=O)CC)C1C2 BLBJUGKATXCWET-UHFFFAOYSA-N 0.000 claims description 3
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 claims description 3
NMXZJPNAJUDMAC-UHFFFAOYSA-N decyl 2-aminobenzoate Chemical compound CCCCCCCCCCOC(=O)C1=CC=CC=C1N NMXZJPNAJUDMAC-UHFFFAOYSA-N 0.000 claims description 3
NUCJYHHDSCEKQN-UHFFFAOYSA-M dimethyl-bis(2-octadecanoyloxyethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC(=O)OCC[N+](C)(C)CCOC(=O)CCCCCCCCCCCCCCCCC NUCJYHHDSCEKQN-UHFFFAOYSA-M 0.000 claims description 3
CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 claims description 3
KRCQDQXKPOKJOE-WLNWXRDVSA-N ethyl (2e,4e,7e)-deca-2,4,7-trienoate Chemical compound CCOC(=O)\C=C\C=C\C\C=C\CC KRCQDQXKPOKJOE-WLNWXRDVSA-N 0.000 claims description 3
229940067592 ethyl palmitate Drugs 0.000 claims description 3
IBIDUABZZSJJNF-UHFFFAOYSA-N furan-2-ylmethyl hexanoate Chemical compound CCCCCC(=O)OCC1=CC=CO1 IBIDUABZZSJJNF-UHFFFAOYSA-N 0.000 claims description 3
YDVXYTIIPGKIJP-NTCAYCPXSA-N geranyl benzoate Chemical compound CC(C)=CCC\C(C)=C\COC(=O)C1=CC=CC=C1 YDVXYTIIPGKIJP-NTCAYCPXSA-N 0.000 claims description 3
150000004676 glycans Chemical class 0.000 claims description 3
GOKKOFHHJFGZHW-UHFFFAOYSA-N hexyl propanoate Chemical compound CCCCCCOC(=O)CC GOKKOFHHJFGZHW-UHFFFAOYSA-N 0.000 claims description 3
239000001174 methyl (E)-non-2-enoate Substances 0.000 claims description 3
NVAGRWXDIIKUBU-UHFFFAOYSA-N methyl 2,6,6-trimethylcyclohex-2-ene-1-carboxylate Chemical compound COC(=O)C1C(C)=CCCC1(C)C NVAGRWXDIIKUBU-UHFFFAOYSA-N 0.000 claims description 3
WTTJVINHCBCLGX-NQLNTKRDSA-N methyl linoleate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OC WTTJVINHCBCLGX-NQLNTKRDSA-N 0.000 claims description 3
BOPPSUHPZARXTH-UHFFFAOYSA-N ocean propanal Chemical compound O=CC(C)CC1=CC=C2OCOC2=C1 BOPPSUHPZARXTH-UHFFFAOYSA-N 0.000 claims description 3
QKNZNUNCDJZTCH-UHFFFAOYSA-N pentyl benzoate Chemical compound CCCCCOC(=O)C1=CC=CC=C1 QKNZNUNCDJZTCH-UHFFFAOYSA-N 0.000 claims description 3
JDQVBGQWADMTAM-UHFFFAOYSA-N phenethyl isobutyrate Chemical compound CC(C)C(=O)OCCC1=CC=CC=C1 JDQVBGQWADMTAM-UHFFFAOYSA-N 0.000 claims description 3
229920001282 polysaccharide Polymers 0.000 claims description 3
239000005017 polysaccharide Substances 0.000 claims description 3
229920005573 silicon-containing polymer Polymers 0.000 claims description 3
239000002689 soil Substances 0.000 claims description 3
239000003381 stabilizer Substances 0.000 claims description 3
CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 claims description 3
238000012546 transfer Methods 0.000 claims description 3
MEAGMJILPLJCFQ-UHFFFAOYSA-N tricyclo[5.2.1.02,6]dec-3-en-8-yl pivalate Chemical compound C12CC=CC2C2CC(OC(=O)C(C)(C)C)C1C2 MEAGMJILPLJCFQ-UHFFFAOYSA-N 0.000 claims description 3
NRZJSHMHHFWKBV-UHFFFAOYSA-N undec-10-enenitrile Chemical compound C=CCCCCCCCCC#N NRZJSHMHHFWKBV-UHFFFAOYSA-N 0.000 claims description 3
AYXPYQRXGNDJFU-IMNVLQEYSA-N viridiflorol Chemical compound [C@@H]1([C@@](CC[C@@H]2[C@H]3C2(C)C)(C)O)[C@H]3[C@H](C)CC1 AYXPYQRXGNDJFU-IMNVLQEYSA-N 0.000 claims description 3
WGPCZPLRVAWXPW-UHFFFAOYSA-N xi-Dihydro-5-octyl-2(3H)-furanone Chemical compound CCCCCCCCC1CCC(=O)O1 WGPCZPLRVAWXPW-UHFFFAOYSA-N 0.000 claims description 3
ADIDQIZBYUABQK-UHFFFAOYSA-N α-guaiene Chemical compound C1C(C(C)=C)CCC(C)C2=C1C(C)CC2 ADIDQIZBYUABQK-UHFFFAOYSA-N 0.000 claims description 3
KWFJIXPIFLVMPM-UHFFFAOYSA-N α-santalene Chemical compound C1C2C3(C)C2CC1C3(C)CCC=C(C)C KWFJIXPIFLVMPM-UHFFFAOYSA-N 0.000 claims description 3
OZQAPQSEYFAMCY-QLFBSQMISA-N α-selinene Chemical compound C1CC=C(C)[C@@H]2C[C@H](C(=C)C)CC[C@]21C OZQAPQSEYFAMCY-QLFBSQMISA-N 0.000 claims description 3
LFJQCDVYDGGFCH-UHFFFAOYSA-N β-phellandrene Chemical compound CC(C)C1CCC(=C)C=C1 LFJQCDVYDGGFCH-UHFFFAOYSA-N 0.000 claims description 3
ZHWLEUGSDGROJS-UHFFFAOYSA-N (2-tert-butylcyclohexyl) ethyl carbonate Chemical compound CCOC(=O)OC1CCCCC1C(C)(C)C ZHWLEUGSDGROJS-UHFFFAOYSA-N 0.000 claims description 2
239000001112 (2E)-1,1-diethoxy-3,7-dimethylocta-2,6-diene Substances 0.000 claims description 2
HZYHMHHBBBSGHB-DYWGDJMRSA-N (2e,6e)-nona-2,6-dienal Chemical compound CC\C=C\CC\C=C\C=O HZYHMHHBBBSGHB-DYWGDJMRSA-N 0.000 claims description 2
MXIGGIZQUGDKAP-UHFFFAOYSA-N (4-methyl-4-phenylpentan-2-yl) acetate Chemical compound CC(=O)OC(C)CC(C)(C)C1=CC=CC=C1 MXIGGIZQUGDKAP-UHFFFAOYSA-N 0.000 claims description 2
QLRNLHNEZFMRSR-SOFGYWHQSA-N (4e)-3,7-dimethylocta-4,6-dien-3-ol Chemical compound CCC(C)(O)\C=C\C=C(C)C QLRNLHNEZFMRSR-SOFGYWHQSA-N 0.000 claims description 2
239000001496 (E)-2-methyl-3-phenylprop-2-enal Substances 0.000 claims description 2
SGRPYYYZQSBLEY-DWJQMLCTSA-N (Z)-1-but-2-enoxyhex-3-ene Chemical compound C(C=CC)OCC\C=C/CC SGRPYYYZQSBLEY-DWJQMLCTSA-N 0.000 claims description 2
QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 claims description 2
YWVSYRJWCROMKO-UHFFFAOYSA-N 1-(3,3-dimethylcyclohexyl)ethyl acetate Chemical compound CC(=O)OC(C)C1CCCC(C)(C)C1 YWVSYRJWCROMKO-UHFFFAOYSA-N 0.000 claims description 2
NFASPEPDTMCBEN-UHFFFAOYSA-N 1-(3,3-dimethylcyclohexyl)ethyl formate Chemical compound O=COC(C)C1CCCC(C)(C)C1 NFASPEPDTMCBEN-UHFFFAOYSA-N 0.000 claims description 2
NEHPIUGJDUWSRR-UHFFFAOYSA-N 1-(4-propan-2-ylcyclohexyl)ethanol Chemical compound CC(C)C1CCC(C(C)O)CC1 NEHPIUGJDUWSRR-UHFFFAOYSA-N 0.000 claims description 2
KDPSHFVSTJYAJQ-UHFFFAOYSA-N 1-ethoxy-4-(2-methylbutan-2-yl)cyclohexane Chemical compound CCOC1CCC(C(C)(C)CC)CC1 KDPSHFVSTJYAJQ-UHFFFAOYSA-N 0.000 claims description 2
PUKWIVZFEZFVAT-UHFFFAOYSA-N 2,2,5-trimethyl-5-pentylcyclopentan-1-one Chemical compound CCCCCC1(C)CCC(C)(C)C1=O PUKWIVZFEZFVAT-UHFFFAOYSA-N 0.000 claims description 2
SHWFPOIJJLMZKA-UHFFFAOYSA-N 2,4-dimethyl-4,4a,5,9b-tetrahydroindeno[1,2-d][1,3]dioxine Chemical compound C1=CC=C2C3OC(C)OC(C)C3CC2=C1 SHWFPOIJJLMZKA-UHFFFAOYSA-N 0.000 claims description 2
HBNHCGDYYBMKJN-UHFFFAOYSA-N 2-(4-methylcyclohexyl)propan-2-yl acetate Chemical compound CC1CCC(C(C)(C)OC(C)=O)CC1 HBNHCGDYYBMKJN-UHFFFAOYSA-N 0.000 claims description 2
SJWKGDGUQTWDRV-UHFFFAOYSA-N 2-Propenyl heptanoate Chemical compound CCCCCCC(=O)OCC=C SJWKGDGUQTWDRV-UHFFFAOYSA-N 0.000 claims description 2
VHBOIZSCWFNPBM-UHFFFAOYSA-N 2-[(4-methylphenyl)methylidene]heptanal Chemical compound CCCCCC(C=O)=CC1=CC=C(C)C=C1 VHBOIZSCWFNPBM-UHFFFAOYSA-N 0.000 claims description 2
UKLOORXNVRHFRM-UHFFFAOYSA-N 2-benzyl-2-methylbut-3-enenitrile Chemical compound C=CC(C#N)(C)CC1=CC=CC=C1 UKLOORXNVRHFRM-UHFFFAOYSA-N 0.000 claims description 2
RQXTZKGDMNIWJF-UHFFFAOYSA-N 2-butan-2-ylcyclohexan-1-one Chemical compound CCC(C)C1CCCCC1=O RQXTZKGDMNIWJF-UHFFFAOYSA-N 0.000 claims description 2
DRTBYQJIHFSKDT-UHFFFAOYSA-N 2-methyl-5-phenylpentan-1-ol Chemical compound OCC(C)CCCC1=CC=CC=C1 DRTBYQJIHFSKDT-UHFFFAOYSA-N 0.000 claims description 2
QNBZQCMSRGAZCR-UHFFFAOYSA-N 2-prop-2-enoxyethylbenzene Chemical compound C=CCOCCC1=CC=CC=C1 QNBZQCMSRGAZCR-UHFFFAOYSA-N 0.000 claims description 2
FAGYGFPZNTYLAO-UHFFFAOYSA-N 3,7-dimethyl-2-methylideneoct-6-enal Chemical compound O=CC(=C)C(C)CCC=C(C)C FAGYGFPZNTYLAO-UHFFFAOYSA-N 0.000 claims description 2
UWKAYLJWKGQEPM-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl acetate Chemical compound CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 claims description 2
HLCSDJLATUNSSI-UHFFFAOYSA-N 3,7-dimethylocta-2,6-dienenitrile Chemical compound CC(C)=CCCC(C)=CC#N HLCSDJLATUNSSI-UHFFFAOYSA-N 0.000 claims description 2
RBKRCARRXLFUGJ-UHFFFAOYSA-N 3,7-dimethyloctan-3-yl acetate Chemical compound CC(=O)OC(C)(CC)CCCC(C)C RBKRCARRXLFUGJ-UHFFFAOYSA-N 0.000 claims description 2
BARWQAWUANUTNS-UHFFFAOYSA-N 3-methoxy-3,7-dimethylocta-1,6-diene Chemical compound COC(C)(C=C)CCC=C(C)C BARWQAWUANUTNS-UHFFFAOYSA-N 0.000 claims description 2
WXCMHFPAUCOJIG-UHFFFAOYSA-N 4'-tert-Butyl-2',6'-dimethyl-3',5'-dinitroacetophenone Chemical compound CC(=O)C1=C(C)C([N+]([O-])=O)=C(C(C)(C)C)C([N+]([O-])=O)=C1C WXCMHFPAUCOJIG-UHFFFAOYSA-N 0.000 claims description 2
YWJHQHJWHJRTAB-UHFFFAOYSA-N 4-(2-Methoxypropan-2-yl)-1-methylcyclohex-1-ene Chemical compound COC(C)(C)C1CCC(C)=CC1 YWJHQHJWHJRTAB-UHFFFAOYSA-N 0.000 claims description 2
VDQZABQVXYELSI-UHFFFAOYSA-N 4-(2-methylbutan-2-yl)cyclohexan-1-ol Chemical compound CCC(C)(C)C1CCC(O)CC1 VDQZABQVXYELSI-UHFFFAOYSA-N 0.000 claims description 2
GDAVABNCFOTAOD-UHFFFAOYSA-N 4-methyl-2-phenyloxane Chemical compound C1C(C)CCOC1C1=CC=CC=C1 GDAVABNCFOTAOD-UHFFFAOYSA-N 0.000 claims description 2
VEZKFOIEZCNFBT-UHFFFAOYSA-N 5-methyl-5-phenylhexan-3-one Chemical compound CCC(=O)CC(C)(C)C1=CC=CC=C1 VEZKFOIEZCNFBT-UHFFFAOYSA-N 0.000 claims description 2
HDQVGGOVPFQTRB-UHFFFAOYSA-N 6,8-dimethylnonan-2-ol Chemical compound CC(C)CC(C)CCCC(C)O HDQVGGOVPFQTRB-UHFFFAOYSA-N 0.000 claims description 2
NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 claims description 2
DZNVIZQPWLDQHI-UHFFFAOYSA-N Citronellyl formate Chemical compound O=COCCC(C)CCC=C(C)C DZNVIZQPWLDQHI-UHFFFAOYSA-N 0.000 claims description 2
239000005770 Eugenol Substances 0.000 claims description 2
241000134874 Geraniales Species 0.000 claims description 2
FHLGUOHLUFIAAA-UHFFFAOYSA-N Linalyl butyrate Chemical compound CCCC(=O)OC(C)(C=C)CCC=C(C)C FHLGUOHLUFIAAA-UHFFFAOYSA-N 0.000 claims description 2
KMRMUZKLFIEVAO-RKDXNWHRSA-N Myrtenal Natural products C1[C@H]2C(C)(C)[C@@H]1CC=C2C=O KMRMUZKLFIEVAO-RKDXNWHRSA-N 0.000 claims description 2
239000006057 Non-nutritive feed additive Substances 0.000 claims description 2
YDVXYTIIPGKIJP-UHFFFAOYSA-N O-Benzoyl-geraniol Natural products CC(C)=CCCC(C)=CCOC(=O)C1=CC=CC=C1 YDVXYTIIPGKIJP-UHFFFAOYSA-N 0.000 claims description 2
UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 claims description 2
YYBMOGCOPQVSLQ-SAPNQHFASA-N [(2e)-3,7-dimethylocta-2,6-dienyl] octanoate Chemical compound CCCCCCCC(=O)OC\C=C(/C)CCC=C(C)C YYBMOGCOPQVSLQ-SAPNQHFASA-N 0.000 claims description 2
FQMZVFJYMPNUCT-XFFZJAGNSA-N [(2z)-3,7-dimethylocta-2,6-dienyl] formate Chemical compound CC(C)=CCC\C(C)=C/COC=O FQMZVFJYMPNUCT-XFFZJAGNSA-N 0.000 claims description 2
JNWQKXUWZWKUAY-XYLIHAQWSA-N [(e)-hex-3-enyl] (e)-2-methylbut-2-enoate Chemical compound CC\C=C\CCOC(=O)C(\C)=C\C JNWQKXUWZWKUAY-XYLIHAQWSA-N 0.000 claims description 2
ZCZSIDMEHXZRLG-UHFFFAOYSA-N acetic acid heptyl ester Natural products CCCCCCCOC(C)=O ZCZSIDMEHXZRLG-UHFFFAOYSA-N 0.000 claims description 2
239000012190 activator Substances 0.000 claims description 2
JKRWZLOCPLZZEI-UHFFFAOYSA-N alpha-Trichloromethylbenzyl acetate Chemical compound CC(=O)OC(C(Cl)(Cl)Cl)C1=CC=CC=C1 JKRWZLOCPLZZEI-UHFFFAOYSA-N 0.000 claims description 2
YMBFCQPIMVLNIU-UHFFFAOYSA-N alpha-bergamotene Chemical compound C1C2C(CCC=C(C)C)(C)C1CC=C2C YMBFCQPIMVLNIU-UHFFFAOYSA-N 0.000 claims description 2
GUUHFMWKWLOQMM-UHFFFAOYSA-N alpha-n-hexylcinnamic aldehyde Natural products CCCCCCC(C=O)=CC1=CC=CC=C1 GUUHFMWKWLOQMM-UHFFFAOYSA-N 0.000 claims description 2
MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 claims description 2
239000012965 benzophenone Substances 0.000 claims description 2
239000007844 bleaching agent Substances 0.000 claims description 2
239000000969 carrier Substances 0.000 claims description 2
HHTWOMMSBMNRKP-UHFFFAOYSA-N carvacrol Natural products CC(=C)C1=CC=C(C)C(O)=C1 HHTWOMMSBMNRKP-UHFFFAOYSA-N 0.000 claims description 2
239000002738 chelating agent Substances 0.000 claims description 2
229940117916 cinnamic aldehyde Drugs 0.000 claims description 2
KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 claims description 2
XPFTVTFOOTVHIA-ALCCZGGFSA-N cis-3-Hexenyl pentanoate Chemical compound CCCCC(=O)OCC\C=C/CC XPFTVTFOOTVHIA-ALCCZGGFSA-N 0.000 claims description 2
ZCHOPXVYTWUHDS-WAYWQWQTSA-N cis-3-hexenyl butyrate Chemical compound CCCC(=O)OCC\C=C/CC ZCHOPXVYTWUHDS-WAYWQWQTSA-N 0.000 claims description 2
229940043350 citral Drugs 0.000 claims description 2
TUEUDXZEBRMJEV-UWVGGRQHSA-N ethyl (1r,6s)-2,2,6-trimethylcyclohexane-1-carboxylate Chemical compound CCOC(=O)[C@@H]1[C@@H](C)CCCC1(C)C TUEUDXZEBRMJEV-UWVGGRQHSA-N 0.000 claims description 2
PZUDDXJZNSJESK-UHFFFAOYSA-N ethyl 2-cyclohexylpropanoate Chemical compound CCOC(=O)C(C)C1CCCCC1 PZUDDXJZNSJESK-UHFFFAOYSA-N 0.000 claims description 2
229940093468 ethylene brassylate Drugs 0.000 claims description 2
229960002217 eugenol Drugs 0.000 claims description 2
229930002886 farnesol Natural products 0.000 claims description 2
229940043259 farnesol Drugs 0.000 claims description 2
NNRLDGQZIVUQTE-UHFFFAOYSA-N gamma-Terpineol Chemical compound CC(C)=C1CCC(C)(O)CC1 NNRLDGQZIVUQTE-UHFFFAOYSA-N 0.000 claims description 2
YUECNVSODFDKOQ-UHFFFAOYSA-N hexyl 2-methylbutanoate Chemical compound CCCCCCOC(=O)C(C)CC YUECNVSODFDKOQ-UHFFFAOYSA-N 0.000 claims description 2
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
239000003752 hydrotrope Substances 0.000 claims description 2
230000002401 inhibitory effect Effects 0.000 claims description 2
PANBRUWVURLWGY-UHFFFAOYSA-N intreleven aldehyde Natural products CCCCCCCCC=CC=O PANBRUWVURLWGY-UHFFFAOYSA-N 0.000 claims description 2
229930007744 linalool Natural products 0.000 claims description 2
DILOFCBIBDMHAY-UHFFFAOYSA-N methyl 2-(3,4-dimethoxyphenyl)acetate Chemical compound COC(=O)CC1=CC=C(OC)C(OC)=C1 DILOFCBIBDMHAY-UHFFFAOYSA-N 0.000 claims description 2
KKVZAVRSVHUSPL-UHFFFAOYSA-N o-methoxycinnamic aldehyde Natural products COC1=CC=CC=C1C=CC=O KKVZAVRSVHUSPL-UHFFFAOYSA-N 0.000 claims description 2
WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 claims description 2
150000004965 peroxy acids Chemical class 0.000 claims description 2
239000000049 pigment Substances 0.000 claims description 2
SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 claims description 2
229950010765 pivalate Drugs 0.000 claims description 2
MBUYSYKXSMTIPP-UHFFFAOYSA-N prop-2-enyl 2-cyclohexyloxyacetate Chemical compound C=CCOC(=O)COC1CCCCC1 MBUYSYKXSMTIPP-UHFFFAOYSA-N 0.000 claims description 2
229930006696 sabinene Natural products 0.000 claims description 2
ZQDPJFUHLCOCRG-AATRIKPKSA-N trans-3-hexene Chemical compound CC\C=C\CC ZQDPJFUHLCOCRG-AATRIKPKSA-N 0.000 claims description 2
GEPCDOWRWODJEY-UHFFFAOYSA-N 3-(3,3-dimethyl-1,2-dihydroinden-5-yl)propanal Chemical compound C1=C(CCC=O)C=C2C(C)(C)CCC2=C1 GEPCDOWRWODJEY-UHFFFAOYSA-N 0.000 claims 7
ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 0.000 claims 6
ABRIMXGLNHCLIP-SOFGYWHQSA-N (5e)-cyclohexadec-5-en-1-one Chemical compound O=C1CCCCCCCCCC\C=C\CCC1 ABRIMXGLNHCLIP-SOFGYWHQSA-N 0.000 claims 4
JSNRRGGBADWTMC-UHFFFAOYSA-N (6E)-7,11-dimethyl-3-methylene-1,6,10-dodecatriene Chemical compound CC(C)=CCCC(C)=CCCC(=C)C=C JSNRRGGBADWTMC-UHFFFAOYSA-N 0.000 claims 4
239000001454 (E)-dec-4-enal Substances 0.000 claims 4
VUIWFNRBSGUSIN-UHFFFAOYSA-N 1-methyl-4-(4-methylpent-3-enyl)cyclohex-3-ene-1-carbaldehyde Chemical compound CC(C)=CCCC1=CCC(C)(C=O)CC1 VUIWFNRBSGUSIN-UHFFFAOYSA-N 0.000 claims 4
HZZBDZGQPYSOEH-UHFFFAOYSA-N C(C)(=O)OC1CC2C3C=CCC3C1C2(C)C Chemical compound C(C)(=O)OC1CC2C3C=CCC3C1C2(C)C HZZBDZGQPYSOEH-UHFFFAOYSA-N 0.000 claims 4
DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims 4
ONKNPOPIGWHAQC-UHFFFAOYSA-N galaxolide Chemical compound C1OCC(C)C2=C1C=C1C(C)(C)C(C)C(C)(C)C1=C2 ONKNPOPIGWHAQC-UHFFFAOYSA-N 0.000 claims 4
OTTZHAVKAVGASB-UHFFFAOYSA-N hept-2-ene Chemical compound CCCCC=CC OTTZHAVKAVGASB-UHFFFAOYSA-N 0.000 claims 4
WHWDWIHXSPCOKZ-UHFFFAOYSA-N hexahydrofarnesyl acetone Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)=O WHWDWIHXSPCOKZ-UHFFFAOYSA-N 0.000 claims 4
YGWKXXYGDYYFJU-UHFFFAOYSA-N menthofuran Chemical compound C1C(C)CCC2=C1OC=C2C YGWKXXYGDYYFJU-UHFFFAOYSA-N 0.000 claims 4
GYUZHTWCNKINPY-UHFFFAOYSA-N theaspirane Chemical compound O1C(C)CCC21C(C)(C)CCC=C2C GYUZHTWCNKINPY-UHFFFAOYSA-N 0.000 claims 4
FDCRKPAGAMPEAD-UHFFFAOYSA-N (+)-β-himachalene oxide Chemical compound C1CC(C)=CC2C31OC3(C)CCCC2(C)C FDCRKPAGAMPEAD-UHFFFAOYSA-N 0.000 claims 3
FUQAYSQLAOJBBC-DHMWGJHJSA-N (1S,2S,5R,8S)-4,4,8-trimethyltricyclo[6.3.1.02,5]dodecan-1-ol Chemical compound CC1(C[C@@H]2[C@@]3(CCC[C@@](CC[C@@H]12)(C3)C)O)C FUQAYSQLAOJBBC-DHMWGJHJSA-N 0.000 claims 3
ITYNGVSTWVVPIC-NSIINPIOSA-N (1as,4ar,7as,7br)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1ah-cyclopropa[e]azulene Chemical compound C([C@H]1[C@@H]2C1(C)C)CC(=C)[C@H]1[C@@H]2C(C)CC1 ITYNGVSTWVVPIC-NSIINPIOSA-N 0.000 claims 3
WFEISWUNAJPLRX-XOCRRNIPSA-N (4E)-4-[(2S,6S)-8-tricyclo[5.2.1.02,6]decanylidene]butanal Chemical compound C1CC[C@@H]2C3\C(\CC([C@H]12)C3)=C\CCC=O WFEISWUNAJPLRX-XOCRRNIPSA-N 0.000 claims 3
QVEOSYKPYFNQAZ-XYOKQWHBSA-N (4e)-4,8-dimethyldeca-4,9-dienal Chemical compound C=CC(C)CC\C=C(/C)CCC=O QVEOSYKPYFNQAZ-XYOKQWHBSA-N 0.000 claims 3
NIIPDXITZPFFTE-IAQYHMDHSA-N (4r,4ar)-4,4a-dimethyl-6-propan-2-ylidene-4,5,7,8-tetrahydro-3h-naphthalen-2-one Chemical compound C1CC(=C(C)C)C[C@]2(C)[C@H](C)CC(=O)C=C21 NIIPDXITZPFFTE-IAQYHMDHSA-N 0.000 claims 3
ZGEHHVDYDNXYMW-OWOJBTEDSA-N (8e)-cyclohexadec-8-en-1-one Chemical compound O=C1CCCCCCC\C=C\CCCCCC1 ZGEHHVDYDNXYMW-OWOJBTEDSA-N 0.000 claims 3
PANBRUWVURLWGY-MDZDMXLPSA-N (E)-2-undecenal Chemical compound CCCCCCCC\C=C\C=O PANBRUWVURLWGY-MDZDMXLPSA-N 0.000 claims 3
NVIPUOMWGQAOIT-UHFFFAOYSA-N (E)-7-Hexadecen-16-olide Natural products O=C1CCCCCC=CCCCCCCCCO1 NVIPUOMWGQAOIT-UHFFFAOYSA-N 0.000 claims 3
MTVBNJVZZAQKRV-DJTWPOEFSA-N (e)-2-methyl-4-[(1r)-2,2,3-trimethylcyclopent-3-en-1-yl]but-2-en-1-ol Chemical compound OCC(/C)=C/C[C@H]1CC=C(C)C1(C)C MTVBNJVZZAQKRV-DJTWPOEFSA-N 0.000 claims 3
JYSHIBMSOWQTJP-UHFFFAOYSA-N 1,1a-dihydrocyclopropa[a]indene Chemical compound C1=CC=C2C3CC3=CC2=C1 JYSHIBMSOWQTJP-UHFFFAOYSA-N 0.000 claims 3
NXPXSRKTNLZHTR-UHFFFAOYSA-N 2,2,4,4,5,6,6-heptamethyl-3a,5,6a,7,8,9-hexahydro-1h-cyclopenta[d][1]benzofuran Chemical compound CC1(C)C(C)C(C)(C)C2CCCC22CC(C)(C)OC21 NXPXSRKTNLZHTR-UHFFFAOYSA-N 0.000 claims 3
XKBNUXGZLQTQKP-UHFFFAOYSA-N 3,5,5,6,7,8,8-heptamethyl-6,7-dihydronaphthalene-2-carbonitrile Chemical compound N#CC1=C(C)C=C2C(C)(C)C(C)C(C)C(C)(C)C2=C1 XKBNUXGZLQTQKP-UHFFFAOYSA-N 0.000 claims 3
ZSYMJWJGUJZQGM-UHFFFAOYSA-N 3-cyclohexyloxy-4,7,7-trimethylbicyclo[2.2.1]heptane Chemical compound CC1(C)C(C2)CCC1(C)C2OC1CCCCC1 ZSYMJWJGUJZQGM-UHFFFAOYSA-N 0.000 claims 3
239000001647 3-phenylprop-2-enyl 2-methylpropanoate Substances 0.000 claims 3
KRKIAJBQOUBNSE-SAQKRVJRSA-N C(C(C)C)(=O)O[C@@H]1[C@]2(CCC(C1)C2(C)C)C Chemical compound C(C(C)C)(=O)O[C@@H]1[C@]2(CCC(C1)C2(C)C)C KRKIAJBQOUBNSE-SAQKRVJRSA-N 0.000 claims 3
RBAUBIIMPLZNGC-HAHDFKILSA-N C(C)(C)(C)C1=CC=C(C=C1)CC(\C=N/C1=C(C(=O)OC)C=CC=C1)C Chemical compound C(C)(C)(C)C1=CC=C(C=C1)CC(\C=N/C1=C(C(=O)OC)C=CC=C1)C RBAUBIIMPLZNGC-HAHDFKILSA-N 0.000 claims 3
OSWSIHUODDHVHZ-UHFFFAOYSA-N C(CC)(=O)OC1CC2C3C=CCC3C1C2(C)C Chemical compound C(CC)(=O)OC1CC2C3C=CCC3C1C2(C)C OSWSIHUODDHVHZ-UHFFFAOYSA-N 0.000 claims 3
LFHQKYSBKVWWOS-MHCOZEDOSA-N CC12[C@H](CC(CC1)C2(C)C)C1CCC(CC1)O Chemical compound CC12[C@H](CC(CC1)C2(C)C)C1CCC(CC1)O LFHQKYSBKVWWOS-MHCOZEDOSA-N 0.000 claims 3
GZMGSIZLVIFVKF-WQRHYEAKSA-N CC1C(CCC(=C1)C)\C=N/C1=C(C(=O)OC)C=CC=C1 Chemical compound CC1C(CCC(=C1)C)\C=N/C1=C(C(=O)OC)C=CC=C1 GZMGSIZLVIFVKF-WQRHYEAKSA-N 0.000 claims 3
YKSSSKBJDZDZTD-CLTKARDFSA-N Isoeugenol benzyl ether Chemical compound COC1=CC(\C=C/C)=CC=C1OCC1=CC=CC=C1 YKSSSKBJDZDZTD-CLTKARDFSA-N 0.000 claims 3
WWXHHJLRAQGSIG-QUEVPRLRSA-N [(1S,2R,5S,7R,8R)-2,6,6,8-tetramethyl-2-tricyclo[5.3.1.01,5]undecanyl] formate Chemical compound C[C@@H]1CC[C@@]2([C@](CC3)(C)OC=O)[C@@H]3C(C)(C)[C@@H]1C2 WWXHHJLRAQGSIG-QUEVPRLRSA-N 0.000 claims 3
OCLOVRSVPZPWHE-SDQBBNPISA-N [(3z)-4,11,11-trimethyl-8-methylidene-5-bicyclo[7.2.0]undec-3-enyl] acetate Chemical compound C1\C=C(\C)C(OC(=O)C)CCC(=C)C2CC(C)(C)C21 OCLOVRSVPZPWHE-SDQBBNPISA-N 0.000 claims 3
KRKIAJBQOUBNSE-COPLHBTASA-N isobornyl isobutyrate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(C)C)C[C@H]1C2(C)C KRKIAJBQOUBNSE-COPLHBTASA-N 0.000 claims 3
SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 claims 3
HVEOFLOFUBUHEQ-UHFFFAOYSA-N tricyclo[5.2.1.02,6]dec-3-en-8-yl butyrate Chemical compound C12CC=CC2C2CC(OC(=O)CCC)C1C2 HVEOFLOFUBUHEQ-UHFFFAOYSA-N 0.000 claims 3
PDEQKAVEYSOLJX-BJMVGYQFSA-N α-santalol Chemical compound C1C2C3(C)C2CC1C3(C)CC\C=C(CO)/C PDEQKAVEYSOLJX-BJMVGYQFSA-N 0.000 claims 3
BQOFWKZOCNGFEC-BDAKNGLRSA-N (+)-Delta3-carene Chemical compound C1C(C)=CC[C@H]2C(C)(C)[C@@H]12 BQOFWKZOCNGFEC-BDAKNGLRSA-N 0.000 claims 2
WRHGORWNJGOVQY-KKUMJFAQSA-N (+)-gamma-cadinene Chemical compound C1CC(C)=C[C@H]2[C@H](C(C)C)CCC(=C)[C@@H]21 WRHGORWNJGOVQY-KKUMJFAQSA-N 0.000 claims 2
KGEKLUUHTZCSIP-UHFFFAOYSA-N (1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl) acetate Chemical compound C1CC2(C)C(OC(=O)C)CC1C2(C)C KGEKLUUHTZCSIP-UHFFFAOYSA-N 0.000 claims 2
QILMAYXCYBTEDM-HNQUOIGGSA-N (10e)-1-oxacycloheptadec-10-en-2-one Chemical compound O=C1CCCCCCC\C=C\CCCCCCO1 QILMAYXCYBTEDM-HNQUOIGGSA-N 0.000 claims 2
MJBVGUVEKHRPDM-HWKANZROSA-N (11e)-1-oxacycloheptadec-11-en-2-one Chemical compound O=C1CCCCCCCC\C=C\CCCCCO1 MJBVGUVEKHRPDM-HWKANZROSA-N 0.000 claims 2
AGZBJJSLDGWKSU-CSKARUKUSA-N (13e)-1-oxacyclohexadec-13-en-2-one Chemical compound O=C1CCCCCCCCCC\C=C\CCO1 AGZBJJSLDGWKSU-CSKARUKUSA-N 0.000 claims 2
GBLRQXKSCRCLBZ-YVQAASCFSA-N (1R,2S,1'R,2'S)-doxacurium Chemical compound COC1=C(OC)C(OC)=CC(C[C@H]2[N@+](CCC3=C2C(=C(OC)C(OC)=C3)OC)(C)CCCOC(=O)CCC(=O)OCCC[N@@+]2(C)[C@@H](C3=C(OC)C(OC)=C(OC)C=C3CC2)CC=2C=C(OC)C(OC)=C(OC)C=2)=C1 GBLRQXKSCRCLBZ-YVQAASCFSA-N 0.000 claims 2
PHNCACYNYORRNS-YFUQURRKSA-N (1R,4S,9S,10R,13S)-5,5,9,13-tetramethyl-14,16-dioxatetracyclo[11.2.1.01,10.04,9]hexadecane Chemical compound CC1(C)CCC[C@]2(C)[C@H]3CC[C@](C)(O4)OC[C@@]34CC[C@H]21 PHNCACYNYORRNS-YFUQURRKSA-N 0.000 claims 2
FIAKMTRUEKZMNO-TZMCWYRMSA-N (1R,8aR)-1,6-dimethyl-4-propan-2-yl-1,2,3,7,8,8a-hexahydronaphthalene Chemical compound CC(C)C1=C2C=C(C)CC[C@@H]2[C@H](C)CC1 FIAKMTRUEKZMNO-TZMCWYRMSA-N 0.000 claims 2
LHYHMMRYTDARSZ-LJISPDSOSA-N (1r,4s,4as,8as)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2h-naphthalen-1-ol Chemical compound C1CC(C)=C[C@@H]2[C@H](C(C)C)CC[C@@](C)(O)[C@H]21 LHYHMMRYTDARSZ-LJISPDSOSA-N 0.000 claims 2
UWSPWQQZFOSTHS-UHFFFAOYSA-N (2,5-dimethyl-1,3-dihydroinden-2-yl)methanol Chemical compound CC1=CC=C2CC(C)(CO)CC2=C1 UWSPWQQZFOSTHS-UHFFFAOYSA-N 0.000 claims 2
LJOISVFAMDWVFA-DRZSPHRISA-N (2s,5s,6s)-2,6,10,10-tetramethyl-1-oxaspiro[4.5]decan-6-ol Chemical compound O1[C@@H](C)CC[C@@]21[C@](O)(C)CCCC2(C)C LJOISVFAMDWVFA-DRZSPHRISA-N 0.000 claims 2
VHBOIZSCWFNPBM-PTNGSMBKSA-N (2z)-2-[(4-methylphenyl)methylidene]heptanal Chemical compound CCCCC\C(C=O)=C\C1=CC=C(C)C=C1 VHBOIZSCWFNPBM-PTNGSMBKSA-N 0.000 claims 2
GUUHFMWKWLOQMM-QINSGFPZSA-N (2z)-2-benzylideneoctanal Chemical compound CCCCCC\C(C=O)=C\C1=CC=CC=C1 GUUHFMWKWLOQMM-QINSGFPZSA-N 0.000 claims 2
DHJVLXVXNFUSMU-HOLFWZHHSA-N (2z,6e)-3,7-dimethylnona-2,6-dienenitrile Chemical compound CC\C(C)=C\CC\C(C)=C/C#N DHJVLXVXNFUSMU-HOLFWZHHSA-N 0.000 claims 2
DSOXXQLCMAEPEZ-UTUPVWNLSA-N (2z,6e)-nona-2,6-dienenitrile Chemical compound CC\C=C\CC\C=C/C#N DSOXXQLCMAEPEZ-UTUPVWNLSA-N 0.000 claims 2
239000001365 (3E,5E)-undeca-1,3,5-triene Substances 0.000 claims 2
YPZUZOLGGMJZJO-RRCSTGOVSA-N (3ar,5ar,9ar,9br)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1h-benzo[e][1]benzofuran Chemical compound CC([C@H]1CC2)(C)CCC[C@@]1(C)[C@@H]1[C@]2(C)OCC1 YPZUZOLGGMJZJO-RRCSTGOVSA-N 0.000 claims 2
YMCJNTJDSOESFI-NWANDNLSSA-N (4as,6s,9ar)-2,6,9,9-tetramethyl-5-methylidene-4,4a,6,7,8,9a-hexahydro-3h-benzo[7]annulene Chemical compound C=C1[C@@H](C)CCC(C)(C)[C@@H]2C=C(C)CC[C@@H]21 YMCJNTJDSOESFI-NWANDNLSSA-N 0.000 claims 2
JIYIHILAGIZIMD-VQHVLOKHSA-N (4e)-cyclopentadec-4-en-1-one Chemical compound O=C1CCCCCCCCCC\C=C\CC1 JIYIHILAGIZIMD-VQHVLOKHSA-N 0.000 claims 2
PAZWFUGWOAQBJJ-SWZPTJTJSA-N (4e,8e)-4,8,12-trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene Chemical compound C1C\C(C)=C\CCC(/C)=C/CCC2(C)OC21 PAZWFUGWOAQBJJ-SWZPTJTJSA-N 0.000 claims 2
JRQWMYKJVZYCDE-BENRWUELSA-N (4z)-3-methylcyclopentadec-4-en-1-one Chemical compound CC\1CC(=O)CCCCCCCCCC\C=C/1 JRQWMYKJVZYCDE-BENRWUELSA-N 0.000 claims 2
FRFUTKHLLZXSEK-DOMZBBRYSA-N (5r,6r)-6,10-dimethyl-4-propan-2-ylidenespiro[4.5]dec-9-en-8-one Chemical compound C[C@@H]1CC(=O)C=C(C)[C@]11C(=C(C)C)CCC1 FRFUTKHLLZXSEK-DOMZBBRYSA-N 0.000 claims 2
NQBWNECTZUOWID-UHFFFAOYSA-N (E)-cinnamyl (E)-cinnamate Natural products C=1C=CC=CC=1C=CC(=O)OCC=CC1=CC=CC=C1 NQBWNECTZUOWID-UHFFFAOYSA-N 0.000 claims 2
239000001727 (E)-dec-2-enal Substances 0.000 claims 2
XBGUIVFBMBVUEG-PFONDFGASA-N (E)-gamma-bisabolene Chemical compound CC(C)=CCC\C(C)=C1/CCC(C)=CC1 XBGUIVFBMBVUEG-PFONDFGASA-N 0.000 claims 2
239000001381 (E)-non-2-enal Substances 0.000 claims 2
239000001118 (E)-tridec-2-enal Substances 0.000 claims 2
239000001320 (E)-undec-2-enal Substances 0.000 claims 2
VPKMGDRERYMTJX-YXVBKTCISA-N (Z)-1-[(1R)-2,6,6-trimethylcyclohex-2-en-1-yl]pent-1-en-3-one Chemical compound CC=1[C@@H](C(CCC=1)(C)C)\C=C/C(CC)=O VPKMGDRERYMTJX-YXVBKTCISA-N 0.000 claims 2
XEJGJTYRUWUFFD-KWZYSKORSA-N (Z)-1-[(1R,2S)-2,6,6-trimethylcyclohex-3-en-1-yl]but-2-en-1-one Chemical compound C[C@@H]1[C@H](C(CC=C1)(C)C)C(\C=C/C)=O XEJGJTYRUWUFFD-KWZYSKORSA-N 0.000 claims 2
YHBUQBJHSRGZNF-AUWJEWJLSA-N (Z)-alpha-bisabolene Chemical compound CC(C)=CC\C=C(\C)C1CCC(C)=CC1 YHBUQBJHSRGZNF-AUWJEWJLSA-N 0.000 claims 2
MTVBNJVZZAQKRV-BJMVGYQFSA-N (e)-2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-en-1-ol Chemical compound OCC(/C)=C/CC1CC=C(C)C1(C)C MTVBNJVZZAQKRV-BJMVGYQFSA-N 0.000 claims 2
QZFSNJAQFWEXEA-MDZDMXLPSA-N (e)-3,3-dimethyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-2-ol Chemical compound CC(O)C(C)(C)\C=C\C1CC=C(C)C1(C)C QZFSNJAQFWEXEA-MDZDMXLPSA-N 0.000 claims 2
RNLHVODSMDJCBR-SOFGYWHQSA-N (e)-3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-2-ol Chemical compound CC(O)C(C)\C=C\C1CC=C(C)C1(C)C RNLHVODSMDJCBR-SOFGYWHQSA-N 0.000 claims 2
ZNWOKRUGFTXKDK-CMDGGOBGSA-N (e)-4-(2,2,3,6-tetramethylcyclohexyl)but-3-en-2-one Chemical compound CC1CCC(C)C(C)(C)C1\C=C\C(C)=O ZNWOKRUGFTXKDK-CMDGGOBGSA-N 0.000 claims 2
IXLLBXDECOMIBP-ALCCZGGFSA-N (z)-1-(2,2-dimethyl-6-methylidenecyclohexyl)but-2-en-1-one Chemical compound C\C=C/C(=O)C1C(=C)CCCC1(C)C IXLLBXDECOMIBP-ALCCZGGFSA-N 0.000 claims 2
KHQDWCKZXLWDNM-GHXNOFRVSA-N (z)-2-ethyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-en-1-ol Chemical compound CC\C(CO)=C\CC1CC=C(C)C1(C)C KHQDWCKZXLWDNM-GHXNOFRVSA-N 0.000 claims 2
QELCXXZZKSRBET-LUAWRHEFSA-N (z)-3-methyl-5-phenylpent-2-enenitrile Chemical compound N#C/C=C(/C)CCC1=CC=CC=C1 QELCXXZZKSRBET-LUAWRHEFSA-N 0.000 claims 2
JZQOJFLIJNRDHK-HJWRWDBZSA-N (z)-4-(2,5,6,6-tetramethylcyclohex-2-en-1-yl)but-3-en-2-one Chemical compound CC1CC=C(C)C(\C=C/C(C)=O)C1(C)C JZQOJFLIJNRDHK-HJWRWDBZSA-N 0.000 claims 2
MMFCJPPRCYDLLZ-HJWRWDBZSA-N (z)-dec-2-enal Chemical compound CCCCCCC\C=C/C=O MMFCJPPRCYDLLZ-HJWRWDBZSA-N 0.000 claims 2
SSNZFFBDIMUILS-KHPPLWFESA-N (z)-dodec-2-enal Chemical compound CCCCCCCCC\C=C/C=O SSNZFFBDIMUILS-KHPPLWFESA-N 0.000 claims 2
HETFMJQWNWIBPN-KTKRTIGZSA-N (z)-undec-2-enenitrile Chemical compound CCCCCCCC\C=C/C#N HETFMJQWNWIBPN-KTKRTIGZSA-N 0.000 claims 2
NTXGFKWLJFHGGJ-UHFFFAOYSA-N 1,1-diethoxy-3,7-dimethylocta-2,6-diene Chemical compound CCOC(OCC)C=C(C)CCC=C(C)C NTXGFKWLJFHGGJ-UHFFFAOYSA-N 0.000 claims 2
NJXYRZMLVYMJHM-UHFFFAOYSA-N 1,1-dimethoxy-2-methylundecane Chemical compound CCCCCCCCCC(C)C(OC)OC NJXYRZMLVYMJHM-UHFFFAOYSA-N 0.000 claims 2
BVDMQAQCEBGIJR-UHFFFAOYSA-N 1-(2,2,6-trimethylcyclohexyl)hexan-3-ol Chemical compound CCCC(O)CCC1C(C)CCCC1(C)C BVDMQAQCEBGIJR-UHFFFAOYSA-N 0.000 claims 2
FXCYGAGBPZQRJE-ZHACJKMWSA-N 1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-1,6-heptadien-3-one Chemical compound CC1=CCCC(C)(C)C1\C=C\C(=O)CCC=C FXCYGAGBPZQRJE-ZHACJKMWSA-N 0.000 claims 2
KUZMAEUMYSXKOU-UHFFFAOYSA-N 1-(2,6,6-trimethylcyclohex-2-en-1-yl)pentan-3-one Chemical compound CCC(=O)CCC1C(C)=CCCC1(C)C KUZMAEUMYSXKOU-UHFFFAOYSA-N 0.000 claims 2
QWAUHUKNKGMBBD-XFIKWOAQSA-N 1-[(2e,5z,9z)-2,6,10-trimethylcyclododeca-2,5,9-trien-1-yl]ethanone Chemical compound CC(=O)C1CC\C(C)=C/CC\C(C)=C/C\C=C1/C QWAUHUKNKGMBBD-XFIKWOAQSA-N 0.000 claims 2
FVUGZKDGWGKCFE-ZBEGNZNMSA-N 1-[(2s,3s)-2,3,8,8-tetramethyl-1,3,4,5,6,7-hexahydronaphthalen-2-yl]ethanone Chemical compound CC1(C)CCCC2=C1C[C@@](C(C)=O)(C)[C@@H](C)C2 FVUGZKDGWGKCFE-ZBEGNZNMSA-N 0.000 claims 2
GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 claims 2
WCOYPFBMFKXWBM-UHFFFAOYSA-N 1-methyl-2-phenoxybenzene Chemical compound CC1=CC=CC=C1OC1=CC=CC=C1 WCOYPFBMFKXWBM-UHFFFAOYSA-N 0.000 claims 2
QQLMXACDDRGTPU-UHFFFAOYSA-N 10-Isopropyl-2,7-dimethyl-1-oxaspiro[4.5]deca-3,6-diene Chemical compound CC(C)C1CCC(C)=CC11C=CC(C)O1 QQLMXACDDRGTPU-UHFFFAOYSA-N 0.000 claims 2
GPVOTKFXWGURGP-UHFFFAOYSA-N 2,5,5-trimethyl-1,3,4,4a,6,7-hexahydronaphthalen-2-ol Chemical compound C1C(C)(O)CCC2C1=CCCC2(C)C GPVOTKFXWGURGP-UHFFFAOYSA-N 0.000 claims 2
BGWAANSABVGTHL-UHFFFAOYSA-N 2,5,5-trimethyl-1,3,4,6,7,8-hexahydronaphthalen-2-ol Chemical compound C1CC(C)(O)CC2=C1C(C)(C)CCC2 BGWAANSABVGTHL-UHFFFAOYSA-N 0.000 claims 2
QSWPBUXWYKVPMT-UHFFFAOYSA-N 2-(5-methyl-2-propan-2-yl-8-bicyclo[2.2.2]oct-5-enyl)-1,3-dioxolane Chemical compound C1C(C=C2C)C(C(C)C)CC2C1C1OCCO1 QSWPBUXWYKVPMT-UHFFFAOYSA-N 0.000 claims 2
BLKPFVWYBFDTPX-UHFFFAOYSA-N 2-(6,6-dimethyl-4-bicyclo[3.1.1]hept-3-enyl)acetaldehyde Chemical compound C1C2C(C)(C)C1CC=C2CC=O BLKPFVWYBFDTPX-UHFFFAOYSA-N 0.000 claims 2
GUMOJENFFHZAFP-UHFFFAOYSA-N 2-Ethoxynaphthalene Chemical compound C1=CC=CC2=CC(OCC)=CC=C21 GUMOJENFFHZAFP-UHFFFAOYSA-N 0.000 claims 2
WZPGQHVPSKTELT-JXMROGBWSA-N 2-Hexylidenecyclopentanone Chemical compound CCCCC\C=C1/CCCC1=O WZPGQHVPSKTELT-JXMROGBWSA-N 0.000 claims 2
AWNOGHRWORTNEI-VXGBXAGGSA-N 2-[(1r,5s)-6,6-dimethyl-4-bicyclo[3.1.1]hept-3-enyl]ethyl acetate Chemical compound CC(=O)OCCC1=CC[C@H]2C(C)(C)[C@@H]1C2 AWNOGHRWORTNEI-VXGBXAGGSA-N 0.000 claims 2
KNHGOYVXAHUDHP-UHFFFAOYSA-N 2-[2-(4-methylcyclohex-3-en-1-yl)propyl]cyclopentan-1-one Chemical compound C1CC(C)=CCC1C(C)CC1CCCC1=O KNHGOYVXAHUDHP-UHFFFAOYSA-N 0.000 claims 2
KSEFBQCEGMTNPD-UHFFFAOYSA-N 2-benzyl-4,4,6-trimethyl-1,3-dioxane Chemical compound O1C(C)CC(C)(C)OC1CC1=CC=CC=C1 KSEFBQCEGMTNPD-UHFFFAOYSA-N 0.000 claims 2
WJWBVJLPGOYBGM-UHFFFAOYSA-N 2-cyclohexylhepta-1,6-dien-3-one Chemical compound C=CCCC(=O)C(=C)C1CCCCC1 WJWBVJLPGOYBGM-UHFFFAOYSA-N 0.000 claims 2
ZHOOOLQOWQVYOE-UHFFFAOYSA-N 2-cyclohexylidene-2-phenylacetonitrile Chemical compound C=1C=CC=CC=1C(C#N)=C1CCCCC1 ZHOOOLQOWQVYOE-UHFFFAOYSA-N 0.000 claims 2
YBGZDTIWKVFICR-RAXLEYEMSA-N 2-ethylhexyl (z)-3-(4-methoxyphenyl)prop-2-enoate Chemical compound CCCCC(CC)COC(=O)\C=C/C1=CC=C(OC)C=C1 YBGZDTIWKVFICR-RAXLEYEMSA-N 0.000 claims 2
YLIXVKUWWOQREC-UHFFFAOYSA-N 2-methyl-3-[4-(2-methylpropyl)phenyl]propanal Chemical compound CC(C)CC1=CC=C(CC(C)C=O)C=C1 YLIXVKUWWOQREC-UHFFFAOYSA-N 0.000 claims 2
CYVGAJHMMVDTDZ-UHFFFAOYSA-N 2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)butan-1-ol Chemical compound OCC(C)CCC1CC=C(C)C1(C)C CYVGAJHMMVDTDZ-UHFFFAOYSA-N 0.000 claims 2
MXNVWZZDDFIWHW-UHFFFAOYSA-N 2-methyl-4-(2,6,6-trimethylcyclohexen-1-yl)butanal Chemical compound O=CC(C)CCC1=C(C)CCCC1(C)C MXNVWZZDDFIWHW-UHFFFAOYSA-N 0.000 claims 2
BSAIUMLZVGUGKX-FPLPWBNLSA-N 2-nonenal Chemical compound CCCCCC\C=C/C=O BSAIUMLZVGUGKX-FPLPWBNLSA-N 0.000 claims 2
VMUNAKQXJLHODT-UHFFFAOYSA-N 2E-tridecenal Natural products CCCCCCCCCCC=CC=O VMUNAKQXJLHODT-UHFFFAOYSA-N 0.000 claims 2
QJXQUYFHUHWIDD-UHFFFAOYSA-N 3,3,6,7-tetramethyl-2,4,4a,5,6,7,8,8a-octahydrochromene Chemical compound C1C(C)(C)COC2CC(C)C(C)CC21 QJXQUYFHUHWIDD-UHFFFAOYSA-N 0.000 claims 2
ZJPKYCLAROITRY-UHFFFAOYSA-N 3-(1-ethoxyethoxy)-3,7-dimethylocta-1,6-diene Chemical compound CCOC(C)OC(C)(C=C)CCC=C(C)C ZJPKYCLAROITRY-UHFFFAOYSA-N 0.000 claims 2
GLZRHVTZLDNUQP-UHFFFAOYSA-N 3-(3-tert-butylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=CC(C(C)(C)C)=C1 GLZRHVTZLDNUQP-UHFFFAOYSA-N 0.000 claims 2
RLEFOSDUWZYGOS-UHFFFAOYSA-N 3-(4-Isopropylphenyl)propanal Chemical compound CC(C)C1=CC=C(CCC=O)C=C1 RLEFOSDUWZYGOS-UHFFFAOYSA-N 0.000 claims 2
NWMCCMGWYCKNJR-UHFFFAOYSA-N 3-(4-ethylphenyl)-2,2-dimethylpropanenitrile Chemical compound CCC1=CC=C(CC(C)(C)C#N)C=C1 NWMCCMGWYCKNJR-UHFFFAOYSA-N 0.000 claims 2
GVSTVIASYRSHQM-UHFFFAOYSA-N 3-(6,6-dimethyl-4-bicyclo[3.1.1]hept-3-enyl)-2,2-dimethylpropanal Chemical compound O=CC(C)(C)CC1=CCC2C(C)(C)C1C2 GVSTVIASYRSHQM-UHFFFAOYSA-N 0.000 claims 2
DDFGFKGJBOILQZ-UHFFFAOYSA-N 3-(6,6-dimethyl-4-bicyclo[3.1.1]hept-3-enyl)propanal Chemical compound C1C2C(C)(C)C1CC=C2CCC=O DDFGFKGJBOILQZ-UHFFFAOYSA-N 0.000 claims 2
NGYMOTOXXHCHOC-UHFFFAOYSA-N 3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pentan-2-ol Chemical compound CC(O)C(C)CCC1CC=C(C)C1(C)C NGYMOTOXXHCHOC-UHFFFAOYSA-N 0.000 claims 2
239000001636 3-phenylprop-2-enyl 3-phenylprop-2-enoate Substances 0.000 claims 2
SIARUXURUGLXOZ-UHFFFAOYSA-N 3a,4,5,6,7,7a-hexahydromethoxy-4,7-methano-1h-indene Chemical compound C1CC2C3C(OC)C=CC3C1C2 SIARUXURUGLXOZ-UHFFFAOYSA-N 0.000 claims 2
FIGQXHMXVPBTDV-UHFFFAOYSA-N 4',7',7'-trimethyl-2-propan-2-ylspiro[1,3-dioxane-4,3'-bicyclo[2.2.1]heptane] Chemical compound O1C(C(C)C)OCCC11C(C2(C)C)(C)CCC2C1 FIGQXHMXVPBTDV-UHFFFAOYSA-N 0.000 claims 2
YLNYLLVKHRZLGO-UHFFFAOYSA-N 4-(1-ethoxyethenyl)-3,3,5,5-tetramethylcyclohexan-1-one Chemical compound CCOC(=C)C1C(C)(C)CC(=O)CC1(C)C YLNYLLVKHRZLGO-UHFFFAOYSA-N 0.000 claims 2
YLVMNUKZYAGOOK-UHFFFAOYSA-N 4-(4-methylpent-3-enyl)cyclohex-3-ene-1-carbonitrile Chemical compound CC(C)=CCCC1=CCC(C#N)CC1 YLVMNUKZYAGOOK-UHFFFAOYSA-N 0.000 claims 2
IKTHMQYJOWTSJO-UHFFFAOYSA-N 4-Acetyl-6-tert-butyl-1,1-dimethylindane Chemical compound CC(=O)C1=CC(C(C)(C)C)=CC2=C1CCC2(C)C IKTHMQYJOWTSJO-UHFFFAOYSA-N 0.000 claims 2
OVJCOXQJBRJIRJ-OVCLIPMQSA-N 4-[(3e)-4,8-dimethylnona-3,7-dienyl]pyridine Chemical compound CC(C)=CCC\C(C)=C\CCC1=CC=NC=C1 OVJCOXQJBRJIRJ-OVCLIPMQSA-N 0.000 claims 2
SWOPLXXJAVYFPY-UHFFFAOYSA-N 4-methyl-2-phenyl-3,6-dihydro-2h-pyran Chemical compound C1C(C)=CCOC1C1=CC=CC=C1 SWOPLXXJAVYFPY-UHFFFAOYSA-N 0.000 claims 2
UJUXUEKQHBXUEM-AATRIKPKSA-N 5-Decenoic acid Chemical compound CCCC\C=C\CCCC(O)=O UJUXUEKQHBXUEM-AATRIKPKSA-N 0.000 claims 2
XNRLAEXLQFIKEY-UHFFFAOYSA-N 5-Hexyldihydro-4-methyl-2(3H)-furanone Chemical compound CCCCCCC1OC(=O)CC1C XNRLAEXLQFIKEY-UHFFFAOYSA-N 0.000 claims 2
DASQRZJTRKBKPP-UHFFFAOYSA-N 5-butan-2-yl-2-(2,4-dimethylcyclohex-3-en-1-yl)-5-methyl-1,3-dioxane Chemical compound O1CC(C(C)CC)(C)COC1C1C(C)C=C(C)CC1 DASQRZJTRKBKPP-UHFFFAOYSA-N 0.000 claims 2
LUNAXRIJWWBQTE-UHFFFAOYSA-N 6-ethoxy-2,2,6-trimethyl-9-methylidenebicyclo[3.3.1]nonane Chemical compound C=C1C2C(OCC)(C)CCC1C(C)(C)CC2 LUNAXRIJWWBQTE-UHFFFAOYSA-N 0.000 claims 2
NJQDALIDWNJDSW-UHFFFAOYSA-N 7,7,8,9,9-pentamethyl-4,4a,5,6,8,9b-hexahydrocyclopenta[h][1,3]benzodioxine Chemical compound O1COCC2CCC(C(C)(C)C(C3(C)C)C)=C3C21 NJQDALIDWNJDSW-UHFFFAOYSA-N 0.000 claims 2
AQJANVUPNABWRU-UHFFFAOYSA-N 8,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalene-2-carbaldehyde Chemical compound C1C(C=O)CCC2=C1C(C)(C)CCC2 AQJANVUPNABWRU-UHFFFAOYSA-N 0.000 claims 2
NKDJGNROVOPIGT-UHFFFAOYSA-N 8,8-dimethyl-9-propan-2-yl-6,10-dioxaspiro[4.5]decane Chemical compound O1CC(C)(C)C(C(C)C)OC11CCCC1 NKDJGNROVOPIGT-UHFFFAOYSA-N 0.000 claims 2
FMYCPRQGKSONCP-UHFFFAOYSA-N Acetal R Chemical compound CCCOC(C)OCCC1=CC=CC=C1 FMYCPRQGKSONCP-UHFFFAOYSA-N 0.000 claims 2
SEJOGXDJLQTMBH-ITGHMWBKSA-N C(C)(C)[C@@H]1CC[C@H]([C@]23[C@H]1[C@H]2C=CC3)C Chemical compound C(C)(C)[C@@H]1CC[C@H]([C@]23[C@H]1[C@H]2C=CC3)C SEJOGXDJLQTMBH-ITGHMWBKSA-N 0.000 claims 2
HJEFAEQTNTXLHL-NNYUYHANSA-N C(C)(C)[C@H]1[C@@H]([C@H]2C=C[C@H]1C2)C(=O)OCC Chemical compound C(C)(C)[C@H]1[C@@H]([C@H]2C=C[C@H]1C2)C(=O)OCC HJEFAEQTNTXLHL-NNYUYHANSA-N 0.000 claims 2
PDUFSBFWOJELLV-RYUDHWBXSA-N C(CC)(=O)OCC(=O)O[C@@H](C)[C@@H]1CC(CCC1)(C)C Chemical compound C(CC)(=O)OCC(=O)O[C@@H](C)[C@@H]1CC(CCC1)(C)C PDUFSBFWOJELLV-RYUDHWBXSA-N 0.000 claims 2
WLYRYWQOUXKANL-FJPHMEQPSA-N C/C(/C(=O)O\C=C/CCCC)=C/C Chemical compound C/C(/C(=O)O\C=C/CCCC)=C/C WLYRYWQOUXKANL-FJPHMEQPSA-N 0.000 claims 2
JJHZLPJQTHPGEI-XFFZJAGNSA-N C/C(/C=O)=C/CC1C(=CCCC1(C)C)C Chemical compound C/C(/C=O)=C/CC1C(=CCCC1(C)C)C JJHZLPJQTHPGEI-XFFZJAGNSA-N 0.000 claims 2
CFYWBOZLQRYGSN-DEPILCGCSA-N CC(O)C(C)\C=C1/C[C@H]2C[C@@H]1[C@@H]1C=CC[C@H]21 Chemical compound CC(O)C(C)\C=C1/C[C@H]2C[C@@H]1[C@@H]1C=CC[C@H]21 CFYWBOZLQRYGSN-DEPILCGCSA-N 0.000 claims 2
SFEOKXHPFMOVRM-FPLPWBNLSA-N CC1(C(C(CCC1)=C)\C=C/C(C)=O)C Chemical compound CC1(C(C(CCC1)=C)\C=C/C(C)=O)C SFEOKXHPFMOVRM-FPLPWBNLSA-N 0.000 claims 2
HOOIQKXOCWQNMI-QWHCGFSZSA-N CC1=CC[C@@H](CC1)[C@@](C)(CCC=C)O Chemical compound CC1=CC[C@@H](CC1)[C@@](C)(CCC=C)O HOOIQKXOCWQNMI-QWHCGFSZSA-N 0.000 claims 2
WXQGPFZDVCRBME-JEIKQXNFSA-N CC1=CC[C@@]2(CCCC(C22[C@@H]1C2)(C)C)C Chemical compound CC1=CC[C@@]2(CCCC(C22[C@@H]1C2)(C)C)C WXQGPFZDVCRBME-JEIKQXNFSA-N 0.000 claims 2
NAMUVRSTEVMHAJ-WOJGMQOQSA-N CC=1CC(CC(C=1)C)\C=N\C1=C(C(=O)OC)C=CC=C1 Chemical compound CC=1CC(CC(C=1)C)\C=N\C1=C(C(=O)OC)C=CC=C1 NAMUVRSTEVMHAJ-WOJGMQOQSA-N 0.000 claims 2
BFBPISPWJZMWJN-CPNJWEJPSA-N COC(=O)C1=CC=CC=C1\N=C\CC(C)CCCC(C)(C)O Chemical compound COC(=O)C1=CC=CC=C1\N=C\CC(C)CCCC(C)(C)O BFBPISPWJZMWJN-CPNJWEJPSA-N 0.000 claims 2
HRGPYCVTDOECMG-VRUQUDLLSA-N CO[C@]1(CC[C@@]23[C@@H](CC[C@H]2C([C@@H]1C3)(C)C)C)C Chemical compound CO[C@]1(CC[C@@]23[C@@H](CC[C@H]2C([C@@H]1C3)(C)C)C)C HRGPYCVTDOECMG-VRUQUDLLSA-N 0.000 claims 2
LFWRAJWJODKLTN-QIBUSXHKSA-N C[C@@H]1C(C[C@@]2(CCCC(C22[C@@H]1C2)(C)C)C)=O Chemical compound C[C@@H]1C(C[C@@]2(CCCC(C22[C@@H]1C2)(C)C)C)=O LFWRAJWJODKLTN-QIBUSXHKSA-N 0.000 claims 2
PFSTYGCNVAVZBK-VCIUYEIQSA-N C\C(CC\C=C(\C)C=O)=C/C\C=C(/C)C=C Chemical compound C\C(CC\C=C(\C)C=O)=C/C\C=C(/C)C=C PFSTYGCNVAVZBK-VCIUYEIQSA-N 0.000 claims 2
JQQDKNVOSLONRS-STRRHFTISA-N Cystophorene Chemical compound CCCCC\C=C/C=C/C=C JQQDKNVOSLONRS-STRRHFTISA-N 0.000 claims 2
239000005697 Dodecan-1-ol Substances 0.000 claims 2
239000005698 Dodecyl acetate Substances 0.000 claims 2
NHJSLVJXXDHDRV-UHFFFAOYSA-N Etaspirene Chemical compound CCC1=CCCC(C)(C)C11C=CC(C)O1 NHJSLVJXXDHDRV-UHFFFAOYSA-N 0.000 claims 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 2
ZGIGZINMAOQWLX-UHFFFAOYSA-N Farnesyl acetate Natural products CC(C)=CCCC(C)=CCCC(C)=CCOC(C)=O ZGIGZINMAOQWLX-UHFFFAOYSA-N 0.000 claims 2
NPNUFJAVOOONJE-FLFDDASRSA-N Isocaryophyllene Chemical compound C1CC(/C)=C\CCC(=C)[C@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-FLFDDASRSA-N 0.000 claims 2
VJYFMQREUJXCQV-UHFFFAOYSA-N Limonene aldehyde Chemical compound O=CCC(C)C1CCC(C)=CC1 VJYFMQREUJXCQV-UHFFFAOYSA-N 0.000 claims 2
OJKMRECJBIPPRG-UHFFFAOYSA-N Linalyl caprylate Chemical compound CCCCCCCC(=O)OC(C)(C=C)CCC=C(C)C OJKMRECJBIPPRG-UHFFFAOYSA-N 0.000 claims 2
ZBJCYZPANVLBRK-UHFFFAOYSA-N Menthone 1,2-glyceryl ketal Chemical compound CC(C)C1CCC(C)CC11OC(CO)CO1 ZBJCYZPANVLBRK-UHFFFAOYSA-N 0.000 claims 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims 2
FAFMZORPAAGQFV-CWSCBRNRSA-N [(1R,2R,4S)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl] propanoate Chemical compound C(CC)(=O)O[C@H]1[C@@]2(CC[C@@H](C1)C2(C)C)C FAFMZORPAAGQFV-CWSCBRNRSA-N 0.000 claims 2
KGEKLUUHTZCSIP-VULFSTHESA-N [(1R,4S)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl] acetate Chemical compound C(C)(=O)OC1[C@@]2(CC[C@@H](C1)C2(C)C)C KGEKLUUHTZCSIP-VULFSTHESA-N 0.000 claims 2
BXGLLMNDXKACMT-JLHYYAGUSA-N [(5e)-6,10-dimethylundeca-5,9-dien-2-yl] acetate Chemical compound CC(=O)OC(C)CC\C=C(/C)CCC=C(C)C BXGLLMNDXKACMT-JLHYYAGUSA-N 0.000 claims 2
BXGLLMNDXKACMT-RAXLEYEMSA-N [(5z)-6,10-dimethylundeca-5,9-dien-2-yl] acetate Chemical compound CC(=O)OC(C)CC\C=C(\C)CCC=C(C)C BXGLLMNDXKACMT-RAXLEYEMSA-N 0.000 claims 2
MPKOLWUWOADQCX-ICFOKQHNSA-N [(Z)-2-(diethoxymethyl)hept-1-enyl]benzene Chemical compound CCCCC\C(=C\C1=CC=CC=C1)C(OCC)OCC MPKOLWUWOADQCX-ICFOKQHNSA-N 0.000 claims 2
UZJQQWFHPLYECS-KQQUZDAGSA-N [(e)-hex-3-enyl] (e)-hex-3-enoate Chemical compound CC\C=C\CCOC(=O)C\C=C\CC UZJQQWFHPLYECS-KQQUZDAGSA-N 0.000 claims 2
BZLYOWSSNHNYKW-UHFFFAOYSA-N [2-[1-(3,3-dimethylcyclohexyl)ethoxy]-2-methylpropyl] cyclopropanecarboxylate Chemical compound C1CCC(C)(C)CC1C(C)OC(C)(C)COC(=O)C1CC1 BZLYOWSSNHNYKW-UHFFFAOYSA-N 0.000 claims 2
LSTSBZKIQFOPHA-UHFFFAOYSA-N [2-[1-(3,3-dimethylcyclohexyl)ethoxy]-2-methylpropyl] propanoate Chemical compound CCC(=O)OCC(C)(C)OC(C)C1CCCC(C)(C)C1 LSTSBZKIQFOPHA-UHFFFAOYSA-N 0.000 claims 2
OEFUEUWVTAXZDS-KWPJZBAWSA-N ac1mhyay Chemical compound C12=CC(=O)CCC2CC2C(C)(C)[C@H]1C2 OEFUEUWVTAXZDS-KWPJZBAWSA-N 0.000 claims 2
CMKQOKAXUWQAHG-UHFFFAOYSA-N alpha-Terpineol propanoate Chemical compound CCC(=O)OC(C)(C)C1CCC(C)=CC1 CMKQOKAXUWQAHG-UHFFFAOYSA-N 0.000 claims 2
YPZUZOLGGMJZJO-LQKXBSAESA-N ambroxan Chemical compound CC([C@@H]1CC2)(C)CCC[C@]1(C)[C@@H]1[C@]2(C)OCC1 YPZUZOLGGMJZJO-LQKXBSAESA-N 0.000 claims 2
NGHOLYJTSCBCGC-QXMHVHEDSA-N benzyl cinnamate Chemical compound C=1C=CC=CC=1\C=C/C(=O)OCC1=CC=CC=C1 NGHOLYJTSCBCGC-QXMHVHEDSA-N 0.000 claims 2
229930006737 car-3-ene Natural products 0.000 claims 2
MIZGSAALSYARKU-UHFFFAOYSA-N cashmeran Chemical compound CC1(C)C(C)C(C)(C)C2=C1C(=O)CCC2 MIZGSAALSYARKU-UHFFFAOYSA-N 0.000 claims 2
RUVINXPYWBROJD-ARJAWSKDSA-N cis-anethole Chemical compound COC1=CC=C(\C=C/C)C=C1 RUVINXPYWBROJD-ARJAWSKDSA-N 0.000 claims 2
CQHUPYQUERYPML-UHFFFAOYSA-N ethyl 2-ethyl-6,6-dimethylcyclohex-2-ene-1-carboxylate Chemical compound CCOC(=O)C1C(CC)=CCCC1(C)C CQHUPYQUERYPML-UHFFFAOYSA-N 0.000 claims 2
ZJLHQWGPVWXKME-UHFFFAOYSA-N ethyl 2-methyl-4-oxo-6-pentylcyclohex-2-ene-1-carboxylate Chemical compound CCCCCC1CC(=O)C=C(C)C1C(=O)OCC ZJLHQWGPVWXKME-UHFFFAOYSA-N 0.000 claims 2
DOVGPJULTGXWJT-UHFFFAOYSA-N ethyl 6,6-dimethyl-2-methylidenecyclohex-3-ene-1-carboxylate Chemical compound CCOC(=O)C1C(=C)C=CCC1(C)C DOVGPJULTGXWJT-UHFFFAOYSA-N 0.000 claims 2
WGPCZPLRVAWXPW-LLVKDONJSA-N gamma-Dodecalactone Natural products CCCCCCCC[C@@H]1CCC(=O)O1 WGPCZPLRVAWXPW-LLVKDONJSA-N 0.000 claims 2
WYTVJTNOJJKEEQ-UHFFFAOYSA-N isospirene Chemical compound C1=CC(C)OC21C(C)=CCC(C)C2C WYTVJTNOJJKEEQ-UHFFFAOYSA-N 0.000 claims 2
SMJXJPQSPQXVMU-UHFFFAOYSA-N methyl 2,2-dimethyl-6-methylidenecyclohexane-1-carboxylate Chemical compound COC(=O)C1C(=C)CCCC1(C)C SMJXJPQSPQXVMU-UHFFFAOYSA-N 0.000 claims 2
OENXQYZXKNBMLM-UHFFFAOYSA-N methyl 2,6,6-trimethylcyclohex-3-ene-1-carboxylate Chemical compound COC(=O)C1C(C)C=CCC1(C)C OENXQYZXKNBMLM-UHFFFAOYSA-N 0.000 claims 2
AEARHBYNCLPVFQ-UHFFFAOYSA-N methyl 2-[(1-hydroxy-3-phenylbutyl)amino]benzoate Chemical compound COC(=O)C1=CC=CC=C1NC(O)CC(C)C1=CC=CC=C1 AEARHBYNCLPVFQ-UHFFFAOYSA-N 0.000 claims 2
125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 2
229940098888 phenethyl benzoate Drugs 0.000 claims 2
WFNDDSQUKATKNX-UHFFFAOYSA-N phenethyl butyrate Chemical compound CCCC(=O)OCCC1=CC=CC=C1 WFNDDSQUKATKNX-UHFFFAOYSA-N 0.000 claims 2
UCQHFDKBUHCAFR-UHFFFAOYSA-N sesquithujene Chemical compound CC1=CCC2(C(CCC=C(C)C)C)C1C2 UCQHFDKBUHCAFR-UHFFFAOYSA-N 0.000 claims 2
AIQLNKITFBJPFO-AATRIKPKSA-N trans-3-hexenyl isovalerate Chemical compound CC\C=C\CCOC(=O)CC(C)C AIQLNKITFBJPFO-AATRIKPKSA-N 0.000 claims 2
CRIGTVCBMUKRSL-ALCCZGGFSA-N α-damascone Chemical compound C\C=C/C(=O)C1C(C)=CCCC1(C)C CRIGTVCBMUKRSL-ALCCZGGFSA-N 0.000 claims 2
CXENHBSYCFFKJS-UHFFFAOYSA-N α-farnesene Chemical compound CC(C)=CCCC(C)=CCC=C(C)C=C CXENHBSYCFFKJS-UHFFFAOYSA-N 0.000 claims 2
NOPLRNXKHZRXHT-PVMFERMNSA-N β-sinensal Chemical compound O=CC(\C)=C/CCC(/C)=C/CCC(=C)C=C NOPLRNXKHZRXHT-PVMFERMNSA-N 0.000 claims 2
229930006720 (-)-alpha-pinene Natural products 0.000 claims 1
RDAFFINKUCJOJK-UYIJSCIWSA-N (1z,5e)-cyclodeca-1,5-diene Chemical compound C1CC\C=C/CC\C=C\C1 RDAFFINKUCJOJK-UYIJSCIWSA-N 0.000 claims 1
AEGTXRAMXBTODF-RYUDHWBXSA-N (2s,4s)-2-heptyl-2,4-dimethyl-1,3-dioxolane Chemical compound CCCCCCC[C@@]1(C)OC[C@H](C)O1 AEGTXRAMXBTODF-RYUDHWBXSA-N 0.000 claims 1
HLCSDJLATUNSSI-YFHOEESVSA-N (2z)-3,7-dimethylocta-2,6-dienenitrile Chemical compound CC(C)=CCC\C(C)=C/C#N HLCSDJLATUNSSI-YFHOEESVSA-N 0.000 claims 1
235000011976 (R)-(+)-citronellal Nutrition 0.000 claims 1
IOLQAHFPDADCHJ-POHAHGRESA-N (e)-5-methyl-2-propan-2-ylhex-2-enal Chemical compound CC(C)C\C=C(\C=O)C(C)C IOLQAHFPDADCHJ-POHAHGRESA-N 0.000 claims 1
LMWNGLDCJDIIBR-HJWRWDBZSA-N (z)-1-(2,6,6-trimethylcyclohexen-1-yl)pent-1-en-3-one Chemical compound CCC(=O)\C=C/C1=C(C)CCCC1(C)C LMWNGLDCJDIIBR-HJWRWDBZSA-N 0.000 claims 1
JWCACDSKXWPOFF-UHFFFAOYSA-N 1-methoxydodecane Chemical compound CCCCCCCCCCCCOC JWCACDSKXWPOFF-UHFFFAOYSA-N 0.000 claims 1
JZOCDHMHLGUPFI-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl formate Chemical compound CC(C)=CCCC(C)(C=C)OC=O JZOCDHMHLGUPFI-UHFFFAOYSA-N 0.000 claims 1
VLFBSPUPYFTTNF-UHFFFAOYSA-N 3-(4-methoxyphenyl)-2-methylpropanal Chemical compound COC1=CC=C(CC(C)C=O)C=C1 VLFBSPUPYFTTNF-UHFFFAOYSA-N 0.000 claims 1
HJZLEGIHUQOJBA-UHFFFAOYSA-M 3-cyclohexylpropanoate Chemical compound [O-]C(=O)CCC1CCCCC1 HJZLEGIHUQOJBA-UHFFFAOYSA-M 0.000 claims 1
YCIXWYOBMVNGTB-UHFFFAOYSA-N 3-methyl-2-pentylcyclopent-2-en-1-one Chemical compound CCCCCC1=C(C)CCC1=O YCIXWYOBMVNGTB-UHFFFAOYSA-N 0.000 claims 1
TWXUTZNBHUWMKJ-UHFFFAOYSA-N Allyl cyclohexylpropionate Chemical compound C=CCOC(=O)CCC1CCCCC1 TWXUTZNBHUWMKJ-UHFFFAOYSA-N 0.000 claims 1
QWRGOHMKGNCVAC-HZJYTTRNSA-N C/C(/C(\C=C/C)=O)=C(/C(C)C)\C Chemical compound C/C(/C(\C=C/C)=O)=C(/C(C)C)\C QWRGOHMKGNCVAC-HZJYTTRNSA-N 0.000 claims 1
HPZWSJQQCJZBBG-INZNQPOWSA-N CC(=C)\C=C/C=C(/C)C=C Chemical compound CC(=C)\C=C/C=C(/C)C=C HPZWSJQQCJZBBG-INZNQPOWSA-N 0.000 claims 1
ZHKPHHPTZCTKBE-UHFFFAOYSA-N CC(C#N)(CCC(C)C1=CC=CC=C1)C Chemical compound CC(C#N)(CCC(C)C1=CC=CC=C1)C ZHKPHHPTZCTKBE-UHFFFAOYSA-N 0.000 claims 1
CRDAMVZIKSXKFV-FBXUGWQNSA-N E,E-Farnesol Natural products CC(C)=CCC\C(C)=C/CC\C(C)=C/CO CRDAMVZIKSXKFV-FBXUGWQNSA-N 0.000 claims 1
BTJXBZZBBNNTOV-UHFFFAOYSA-N Linalyl benzoate Chemical compound CC(C)=CCCC(C)(C=C)OC(=O)C1=CC=CC=C1 BTJXBZZBBNNTOV-UHFFFAOYSA-N 0.000 claims 1
WAQIIHCCEMGYKP-UHFFFAOYSA-N Linalyl propionate Chemical compound CCC(=O)OC(C)(C=C)CCC=C(C)C WAQIIHCCEMGYKP-UHFFFAOYSA-N 0.000 claims 1
ATJYGKZBNSHTKQ-UHFFFAOYSA-N N(=O)OC1=C(C(=C(C(=C1C)C)C)ON=O)C(C)(C)C Chemical compound N(=O)OC1=C(C(=C(C(=C1C)C)C)ON=O)C(C)(C)C ATJYGKZBNSHTKQ-UHFFFAOYSA-N 0.000 claims 1
AXMVYSVVTMKQSL-UHFFFAOYSA-N UNPD142122 Natural products OC1=CC=C(C=CC=O)C=C1O AXMVYSVVTMKQSL-UHFFFAOYSA-N 0.000 claims 1
IGODOXYLBBXFDW-NSHDSACASA-N alpha-Terpinyl acetate Natural products CC(=O)OC(C)(C)[C@@H]1CCC(C)=CC1 IGODOXYLBBXFDW-NSHDSACASA-N 0.000 claims 1
IKTRNOZMSJUISH-UHFFFAOYSA-N azulen-4-ol Chemical compound OC1=CC=CC=C2C=CC=C12 IKTRNOZMSJUISH-UHFFFAOYSA-N 0.000 claims 1
229940050390 benzoate Drugs 0.000 claims 1
QZHPTGXQGDFGEN-UHFFFAOYSA-N chromene Chemical compound C1=CC=C2C=C[CH]OC2=C1 QZHPTGXQGDFGEN-UHFFFAOYSA-N 0.000 claims 1
KXGVEGMKQFWNSR-LLQZFEROSA-N deoxycholic acid Chemical compound C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 KXGVEGMKQFWNSR-LLQZFEROSA-N 0.000 claims 1
REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 claims 1
MGQPKOBPXHENPO-LSCVPOLPSA-N ethyl hexahydro-4,7-methanoindane-3a-carboxylate Chemical compound C([C@@H]1C2)C[C@@H]2[C@@]2(C(=O)OCC)[C@@H]1CCC2 MGQPKOBPXHENPO-LSCVPOLPSA-N 0.000 claims 1
JPXGPRBLTIYFQG-UHFFFAOYSA-N heptan-4-yl acetate Chemical compound CCCC(CCC)OC(C)=O JPXGPRBLTIYFQG-UHFFFAOYSA-N 0.000 claims 1
MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 claims 1
MZNHUHNWGVUEAT-YWEYNIOJSA-N hexyl crotonate Chemical compound CCCCCCOC(=O)\C=C/C MZNHUHNWGVUEAT-YWEYNIOJSA-N 0.000 claims 1
YJSUCBQWLKRPDL-UHFFFAOYSA-N isocyclocitral Chemical compound CC1CC(C)=CC(C)C1C=O YJSUCBQWLKRPDL-UHFFFAOYSA-N 0.000 claims 1
ACOBBFVLNKYODD-NTMALXAHSA-N methyl (2z)-3,7-dimethylocta-2,6-dienoate Chemical compound COC(=O)\C=C(\C)CCC=C(C)C ACOBBFVLNKYODD-NTMALXAHSA-N 0.000 claims 1
150000002825 nitriles Chemical class 0.000 claims 1
KVMWYGAYARXPOL-JYOAFUTRSA-N phenethyl tiglate Chemical compound C\C=C(\C)C(=O)OCCC1=CC=CC=C1 KVMWYGAYARXPOL-JYOAFUTRSA-N 0.000 claims 1
IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 claims 1
UOGMZEGKCNHMBF-UHFFFAOYSA-N scentenal Chemical compound C12CC(C=O)CC2C2CC(OC)C1C2 UOGMZEGKCNHMBF-UHFFFAOYSA-N 0.000 claims 1
150000004665 fatty acids Chemical class 0.000 description 73
150000001875 compounds Chemical class 0.000 description 60
238000012360 testing method Methods 0.000 description 45
CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 40
XYHKNCXZYYTLRG-UHFFFAOYSA-N 1h-imidazole-2-carbaldehyde Chemical compound O=CC1=NC=CN1 XYHKNCXZYYTLRG-UHFFFAOYSA-N 0.000 description 34
GWYFCOCPABKNJV-UHFFFAOYSA-M 3-Methylbutanoic acid Natural products CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 34
GWYFCOCPABKNJV-UHFFFAOYSA-N beta-methyl-butyric acid Natural products CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 34
229920001296 polysiloxane Polymers 0.000 description 32
235000019645 odor Nutrition 0.000 description 31
125000000217 alkyl group Chemical group 0.000 description 28
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 27
230000003750 conditioning effect Effects 0.000 description 23
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 22
125000002877 alkyl aryl group Chemical group 0.000 description 21
150000002148 esters Chemical class 0.000 description 20
229940073505 ethyl vanillin Drugs 0.000 description 20
239000000523 sample Substances 0.000 description 20
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 19
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 17
230000008901 benefit Effects 0.000 description 17
150000005690 diesters Chemical class 0.000 description 17
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
150000001450 anions Chemical class 0.000 description 16
239000000047 product Substances 0.000 description 16
229940100515 sorbitan Drugs 0.000 description 16
125000002091 cationic group Chemical group 0.000 description 14
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 14
239000007795 chemical reaction product Substances 0.000 description 13
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 13
125000003107 substituted aryl group Chemical group 0.000 description 13
125000003545 alkoxy group Chemical group 0.000 description 12
125000003118 aryl group Chemical group 0.000 description 12
229910052739 hydrogen Inorganic materials 0.000 description 12
125000000547 substituted alkyl group Chemical group 0.000 description 12
125000004432 carbon atom Chemical group C* 0.000 description 11
230000000670 limiting effect Effects 0.000 description 11
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 10
NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 10
125000002947 alkylene group Chemical group 0.000 description 10
UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 10
239000000178 monomer Substances 0.000 description 10
239000000126 substance Substances 0.000 description 10
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 9
239000000839 emulsion Substances 0.000 description 9
238000010998 test method Methods 0.000 description 9
239000002253 acid Substances 0.000 description 8
235000011187 glycerol Nutrition 0.000 description 8
229960005150 glycerol Drugs 0.000 description 8
229920000223 polyglycerol Polymers 0.000 description 8
125000005415 substituted alkoxy group Chemical group 0.000 description 8
239000003760 tallow Substances 0.000 description 8
238000011282 treatment Methods 0.000 description 8
KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 7
229910052757 nitrogen Inorganic materials 0.000 description 7
239000003921 oil Substances 0.000 description 7
235000019198 oils Nutrition 0.000 description 7
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 6
ZCHHRLHTBGRGOT-SNAWJCMRSA-N 2-Hexen-1-ol Natural products CCC\C=C\CO ZCHHRLHTBGRGOT-SNAWJCMRSA-N 0.000 description 6
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 6
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 6
239000005642 Oleic acid Substances 0.000 description 6
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 6
239000004698 Polyethylene Substances 0.000 description 6
HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 6
125000000732 arylene group Chemical group 0.000 description 6
238000005516 engineering process Methods 0.000 description 6
239000000835 fiber Substances 0.000 description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 6
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 6
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 6
229920000573 polyethylene Polymers 0.000 description 6
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 6
150000003254 radicals Chemical class 0.000 description 6
XVULBTBTFGYVRC-HHUCQEJWSA-N sclareol Chemical compound CC1(C)CCC[C@]2(C)[C@@H](CC[C@](O)(C)C=C)[C@](C)(O)CC[C@H]21 XVULBTBTFGYVRC-HHUCQEJWSA-N 0.000 description 6
RUVINXPYWBROJD-ONEGZZNKSA-N trans-anethole Chemical compound COC1=CC=C(\C=C\C)C=C1 RUVINXPYWBROJD-ONEGZZNKSA-N 0.000 description 6
150000004670 unsaturated fatty acids Chemical class 0.000 description 6
SBRRDWKWIGRYCN-UHFFFAOYSA-N 2h-cyclopenta[g][1]benzofuran Chemical compound C1=CC2=CCOC2=C2C=CC=C21 SBRRDWKWIGRYCN-UHFFFAOYSA-N 0.000 description 5
ABRIMXGLNHCLIP-VURMDHGXSA-N 5-Cyclohexadecenone Chemical compound O=C1CCCCCCCCCC\C=C/CCC1 ABRIMXGLNHCLIP-VURMDHGXSA-N 0.000 description 5
235000021357 Behenic acid Nutrition 0.000 description 5
BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 5
AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 5
229930006000 Sucrose Natural products 0.000 description 5
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 5
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 5
125000005237 alkyleneamino group Chemical group 0.000 description 5
150000001408 amides Chemical class 0.000 description 5
125000000129 anionic group Chemical group 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
125000004122 cyclic group Chemical group 0.000 description 5
IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 5
PGZPBNJYTNQMAX-UHFFFAOYSA-N dimethylazanium;methyl sulfate Chemical compound C[NH2+]C.COS([O-])(=O)=O PGZPBNJYTNQMAX-UHFFFAOYSA-N 0.000 description 5
239000003995 emulsifying agent Substances 0.000 description 5
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
125000001924 fatty-acyl group Chemical group 0.000 description 5
KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 5
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 5
238000005192 partition Methods 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
229920006395 saturated elastomer Polymers 0.000 description 5
239000000600 sorbitol Substances 0.000 description 5
229960002920 sorbitol Drugs 0.000 description 5
239000007858 starting material Substances 0.000 description 5
238000003860 storage Methods 0.000 description 5
239000005720 sucrose Substances 0.000 description 5
229960004793 sucrose Drugs 0.000 description 5
150000003445 sucroses Chemical class 0.000 description 5
239000000725 suspension Substances 0.000 description 5
150000003512 tertiary amines Chemical class 0.000 description 5
BJIOGJUNALELMI-ONEGZZNKSA-N trans-isoeugenol Chemical compound COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 5
235000021122 unsaturated fatty acids Nutrition 0.000 description 5
239000001993 wax Substances 0.000 description 5
FUQAYSQLAOJBBC-PAPYEOQZSA-N β-caryophyllene alcohol Chemical compound C1C[C@](C2)(C)CCC[C@]2(O)[C@H]2CC(C)(C)[C@@H]21 FUQAYSQLAOJBBC-PAPYEOQZSA-N 0.000 description 5
AZOCECCLWFDTAP-RKDXNWHRSA-N (+)-dihydrocarvone Chemical compound C[C@@H]1CC[C@@H](C(C)=C)CC1=O AZOCECCLWFDTAP-RKDXNWHRSA-N 0.000 description 4
ITYNGVSTWVVPIC-DHGKCCLASA-N (-)-allo-Aromadendrene Chemical compound C([C@@H]1[C@H]2C1(C)C)CC(=C)[C@@H]1[C@H]2[C@H](C)CC1 ITYNGVSTWVVPIC-DHGKCCLASA-N 0.000 description 4
WXQGPFZDVCRBME-QEJZJMRPSA-N (-)-thujopsene Chemical compound C([C@@]1(C)CC=C2C)CCC(C)(C)[C@]11[C@H]2C1 WXQGPFZDVCRBME-QEJZJMRPSA-N 0.000 description 4
ZLQADKTVJQXDIG-SNPRPXQTSA-N (1R,6S,9R)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodec-2-ene Chemical compound C1C[C@H](C2)C(C)(C)O[C@]22C(C)=CCC[C@]21C ZLQADKTVJQXDIG-SNPRPXQTSA-N 0.000 description 4
LFWRAJWJODKLTN-GVARAGBVSA-N (1as,2s,4as,8as)-2,4a,8,8-tetramethyl-1a,2,4,5,6,7-hexahydro-1h-cyclopropa[j]naphthalen-3-one Chemical compound CC1(C)CCC[C@@]2(C)CC(=O)[C@@H](C)[C@H]3[C@@]12C3 LFWRAJWJODKLTN-GVARAGBVSA-N 0.000 description 4
ZHHYXNZJDGDGPJ-BSWSSELBSA-N (2e,4e)-nona-2,4-dienal Chemical compound CCCC\C=C\C=C\C=O ZHHYXNZJDGDGPJ-BSWSSELBSA-N 0.000 description 4
YKSSSKBJDZDZTD-XVNBXDOJSA-N (E)-isoeugenyl benzyl ether Chemical compound COC1=CC(\C=C\C)=CC=C1OCC1=CC=CC=C1 YKSSSKBJDZDZTD-XVNBXDOJSA-N 0.000 description 4
ZWKNLRXFUTWSOY-QPJJXVBHSA-N (e)-3-phenylprop-2-enenitrile Chemical compound N#C\C=C\C1=CC=CC=C1 ZWKNLRXFUTWSOY-QPJJXVBHSA-N 0.000 description 4
DCNHQNGFLVPROM-QXMHVHEDSA-N (z)-n,n-dimethyloctadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN(C)C DCNHQNGFLVPROM-QXMHVHEDSA-N 0.000 description 4
XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 4
HGUFODBRKLSHSI-UHFFFAOYSA-N 2,3,7,8-tetrachloro-dibenzo-p-dioxin Chemical compound O1C2=CC(Cl)=C(Cl)C=C2OC2=C1C=C(Cl)C(Cl)=C2 HGUFODBRKLSHSI-UHFFFAOYSA-N 0.000 description 4
OXYRENDGHPGWKV-UHFFFAOYSA-N 3-methyl-5-phenylpentan-1-ol Chemical compound OCCC(C)CCC1=CC=CC=C1 OXYRENDGHPGWKV-UHFFFAOYSA-N 0.000 description 4
WMOPMQRJLLIEJV-UHFFFAOYSA-N 7-epi-gamma-eudesmanol Natural products C1C(C(C)(C)O)CCC2(C)CCCC(C)=C21 WMOPMQRJLLIEJV-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 4
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 4
ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 4
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 4
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 4
KRCZYMFUWVJCLI-UHFFFAOYSA-N Dihydrocarveol Chemical compound CC1CCC(C(C)=C)CC1O KRCZYMFUWVJCLI-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 4
235000021314 Palmitic acid Nutrition 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
239000004902 Softening Agent Substances 0.000 description 4
229920002472 Starch Polymers 0.000 description 4
235000021355 Stearic acid Nutrition 0.000 description 4
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 4
UCTLHLZWKJIXJI-LXIBVNSESA-N [(3s,8r,9s,10r,13s,14s)-17-chloro-16-formyl-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15-decahydro-1h-cyclopenta[a]phenanthren-3-yl] acetate Chemical compound C([C@@H]12)C[C@]3(C)C(Cl)=C(C=O)C[C@H]3[C@@H]1CC=C1[C@]2(C)CC[C@H](OC(=O)C)C1 UCTLHLZWKJIXJI-LXIBVNSESA-N 0.000 description 4
125000002252 acyl group Chemical group 0.000 description 4
NIIPDXITZPFFTE-ABAIWWIYSA-N alpha-Vetivone Chemical compound C1CC(=C(C)C)C[C@@]2(C)[C@H](C)CC(=O)C=C21 NIIPDXITZPFFTE-ABAIWWIYSA-N 0.000 description 4
XUEHVOLRMXNRKQ-KHMAMNHCSA-N alpha-cubebene Chemical compound CC(C)[C@@H]([C@H]12)CC[C@@H](C)[C@]32[C@@H]1C(C)=CC3 XUEHVOLRMXNRKQ-KHMAMNHCSA-N 0.000 description 4
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
229910052782 aluminium Inorganic materials 0.000 description 4
XTKDAFGWCDAMPY-UHFFFAOYSA-N azaperone Chemical compound C1=CC(F)=CC=C1C(=O)CCCN1CCN(C=2N=CC=CC=2)CC1 XTKDAFGWCDAMPY-UHFFFAOYSA-N 0.000 description 4
229940116226 behenic acid Drugs 0.000 description 4
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
150000007942 carboxylates Chemical class 0.000 description 4
150000001735 carboxylic acids Chemical class 0.000 description 4
ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 description 4
238000005094 computer simulation Methods 0.000 description 4
238000011109 contamination Methods 0.000 description 4
WCASXYBKJHWFMY-UHFFFAOYSA-N crotyl alcohol Chemical compound CC=CCO WCASXYBKJHWFMY-UHFFFAOYSA-N 0.000 description 4
NAPSCFZYZVSQHF-UHFFFAOYSA-N dimantine Chemical compound CCCCCCCCCCCCCCCCCCN(C)C NAPSCFZYZVSQHF-UHFFFAOYSA-N 0.000 description 4
229950010007 dimantine Drugs 0.000 description 4
238000005886 esterification reaction Methods 0.000 description 4
235000019441 ethanol Nutrition 0.000 description 4
239000011888 foil Substances 0.000 description 4
235000021588 free fatty acids Nutrition 0.000 description 4
WWULHQLTPGKDAM-UHFFFAOYSA-N gamma-eudesmol Natural products CC(C)C1CC(O)C2(C)CCCC(=C2C1)C WWULHQLTPGKDAM-UHFFFAOYSA-N 0.000 description 4
DFMAXQKDIGCMTL-UHFFFAOYSA-N isopimpinellin Chemical compound O1C(=O)C=CC2=C1C(OC)=C1OC=CC1=C2OC DFMAXQKDIGCMTL-UHFFFAOYSA-N 0.000 description 4
OOYRHNIVDZZGQV-BHPKHCPMSA-N khusimol Chemical compound C=C1C(C)(C)[C@@H](C2)CC[C@]32[C@@H](CO)CC[C@@H]31 OOYRHNIVDZZGQV-BHPKHCPMSA-N 0.000 description 4
239000002736 nonionic surfactant Substances 0.000 description 4
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 4
GGHMUJBZYLPWFD-UHFFFAOYSA-N patchoulialcohol Chemical compound C1CC2(C)C3(O)CCC(C)C2CC1C3(C)C GGHMUJBZYLPWFD-UHFFFAOYSA-N 0.000 description 4
230000008447 perception Effects 0.000 description 4
229920000728 polyester Polymers 0.000 description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
230000008569 process Effects 0.000 description 4
125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 4
235000019698 starch Nutrition 0.000 description 4
239000008117 stearic acid Substances 0.000 description 4
VHOCUJPBKOZGJD-UHFFFAOYSA-N triacontanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O VHOCUJPBKOZGJD-UHFFFAOYSA-N 0.000 description 4
150000005691 triesters Chemical class 0.000 description 4
ULDHMXUKGWMISQ-VIFPVBQESA-N (+)-carvone Chemical compound CC(=C)[C@H]1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-VIFPVBQESA-N 0.000 description 3
BAVONGHXFVOKBV-NXEZZACHSA-N (-)-cis-carveol Chemical compound CC(=C)[C@@H]1CC=C(C)[C@H](O)C1 BAVONGHXFVOKBV-NXEZZACHSA-N 0.000 description 3
DTGKSKDOIYIVQL-MRTMQBJTSA-N (-)-isoborneol Chemical compound C1C[C@@]2(C)[C@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-MRTMQBJTSA-N 0.000 description 3
IJFKZRMIRAVXRK-VQHVLOKHSA-N (5e)-2,6-dimethylocta-5,7-dien-2-ol Chemical compound C=CC(/C)=C/CCC(C)(C)O IJFKZRMIRAVXRK-VQHVLOKHSA-N 0.000 description 3
239000001306 (7E,9E,11E,13E)-pentadeca-7,9,11,13-tetraen-1-ol Substances 0.000 description 3
BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 3
XJWZDXFFNOMMTD-UHFFFAOYSA-N 1-methyl-4-propan-2-ylcyclohex-3-en-1-ol Chemical compound CC(C)C1=CCC(C)(O)CC1 XJWZDXFFNOMMTD-UHFFFAOYSA-N 0.000 description 3
PZLGNBYOMLFUBO-UHFFFAOYSA-N 1-oxaspiro[4.5]deca-3,6-diene Chemical compound C1=CCOC11C=CCCC1 PZLGNBYOMLFUBO-UHFFFAOYSA-N 0.000 description 3
FJJYHTVHBVXEEQ-UHFFFAOYSA-N 2,2-dimethylpropanal Chemical compound CC(C)(C)C=O FJJYHTVHBVXEEQ-UHFFFAOYSA-N 0.000 description 3
CRBZVDLXAIFERF-UHFFFAOYSA-N 2,4,6-trimethoxybenzaldehyde Chemical compound COC1=CC(OC)=C(C=O)C(OC)=C1 CRBZVDLXAIFERF-UHFFFAOYSA-N 0.000 description 3
VUSBHGLIAQXBSW-UHFFFAOYSA-N 2,6-dimethyloct-7-en-4-one Chemical compound CC(C)CC(=O)CC(C)C=C VUSBHGLIAQXBSW-UHFFFAOYSA-N 0.000 description 3
PETRWTHZSKVLRE-UHFFFAOYSA-N 2-Methoxy-4-methylphenol Chemical compound COC1=CC(C)=CC=C1O PETRWTHZSKVLRE-UHFFFAOYSA-N 0.000 description 3
VNWOJVJCRAHBJJ-UHFFFAOYSA-N 2-pentylcyclopentan-1-one Chemical compound CCCCCC1CCCC1=O VNWOJVJCRAHBJJ-UHFFFAOYSA-N 0.000 description 3
WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 3
OPHQOIGEOHXOGX-UHFFFAOYSA-N 3,4,5-trimethoxybenzaldehyde Chemical compound COC1=CC(C=O)=CC(OC)=C1OC OPHQOIGEOHXOGX-UHFFFAOYSA-N 0.000 description 3
NOTCZLKDULMKBR-UHFFFAOYSA-N 3-Methoxy-5-methylphenol Chemical compound COC1=CC(C)=CC(O)=C1 NOTCZLKDULMKBR-UHFFFAOYSA-N 0.000 description 3
XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 3
OIGWAXDAPKFNCQ-UHFFFAOYSA-N 4-isopropylbenzyl alcohol Chemical compound CC(C)C1=CC=C(CO)C=C1 OIGWAXDAPKFNCQ-UHFFFAOYSA-N 0.000 description 3
MUDSDYNRBDKLGK-UHFFFAOYSA-N 4-methylquinoline Chemical compound C1=CC=C2C(C)=CC=NC2=C1 MUDSDYNRBDKLGK-UHFFFAOYSA-N 0.000 description 3
OALYTRUKMRCXNH-UHFFFAOYSA-N 5-pentyloxolan-2-one Chemical compound CCCCCC1CCC(=O)O1 OALYTRUKMRCXNH-UHFFFAOYSA-N 0.000 description 3
LUYISICIYVKBTA-UHFFFAOYSA-N 6-methylquinoline Chemical compound N1=CC=CC2=CC(C)=CC=C21 LUYISICIYVKBTA-UHFFFAOYSA-N 0.000 description 3
GHBSPIPJMLAMEP-UHFFFAOYSA-N 6-pentyloxan-2-one Chemical compound CCCCCC1CCCC(=O)O1 GHBSPIPJMLAMEP-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
SCCDQYPEOIRVGX-UHFFFAOYSA-N Acetyleugenol Chemical compound COC1=CC(CC=C)=CC=C1OC(C)=O SCCDQYPEOIRVGX-UHFFFAOYSA-N 0.000 description 3
235000004977 Brassica sinapistrum Nutrition 0.000 description 3
229920000858 Cyclodextrin Polymers 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
FPCCDPXRNNVUOM-UHFFFAOYSA-N Hydroxycitronellol Chemical compound OCCC(C)CCCC(C)(C)O FPCCDPXRNNVUOM-UHFFFAOYSA-N 0.000 description 3
KRKIAJBQOUBNSE-GYSYKLTISA-N Isobornyl isobutyrate Chemical compound C1C[C@@]2(C)[C@H](OC(=O)C(C)C)C[C@@H]1C2(C)C KRKIAJBQOUBNSE-GYSYKLTISA-N 0.000 description 3
DIRDKDDFAMNBNY-UHFFFAOYSA-N Isopropyl 2-methylbutanoate Chemical compound CCC(C)C(=O)OC(C)C DIRDKDDFAMNBNY-UHFFFAOYSA-N 0.000 description 3
OCWLYWIFNDCWRZ-UHFFFAOYSA-N Methyl (S)-2-Methylbutanoate Chemical compound CCC(C)C(=O)OC OCWLYWIFNDCWRZ-UHFFFAOYSA-N 0.000 description 3
CRZQGDNQQAALAY-UHFFFAOYSA-N Methyl benzeneacetate Chemical compound COC(=O)CC1=CC=CC=C1 CRZQGDNQQAALAY-UHFFFAOYSA-N 0.000 description 3
229910002651 NO3 Inorganic materials 0.000 description 3
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 3
IYTXKIXETAELAV-UHFFFAOYSA-N Nonan-3-one Chemical compound CCCCCCC(=O)CC IYTXKIXETAELAV-UHFFFAOYSA-N 0.000 description 3
ZYEMGPIYFIJGTP-UHFFFAOYSA-N O-methyleugenol Chemical compound COC1=CC=C(CC=C)C=C1OC ZYEMGPIYFIJGTP-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
229920000297 Rayon Polymers 0.000 description 3
125000003342 alkenyl group Chemical group 0.000 description 3
150000003973 alkyl amines Chemical class 0.000 description 3
PDEQKAVEYSOLJX-BKKZDLJQSA-N alpha-santalol Chemical compound C1C2[C@]3(C)C2C[C@H]1[C@@]3(C)CC/C=C(CO)/C PDEQKAVEYSOLJX-BKKZDLJQSA-N 0.000 description 3
125000003368 amide group Chemical group 0.000 description 3
150000003868 ammonium compounds Chemical class 0.000 description 3
239000003945 anionic surfactant Substances 0.000 description 3
239000003963 antioxidant agent Substances 0.000 description 3
235000006708 antioxidants Nutrition 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 3
AKGGYBADQZYZPD-UHFFFAOYSA-N benzylacetone Chemical compound CC(=O)CCC1=CC=CC=C1 AKGGYBADQZYZPD-UHFFFAOYSA-N 0.000 description 3
230000000903 blocking effect Effects 0.000 description 3
238000004364 calculation method Methods 0.000 description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
NVEQFIOZRFFVFW-RGCMKSIDSA-N caryophyllene oxide Chemical compound C=C1CC[C@H]2O[C@]2(C)CC[C@H]2C(C)(C)C[C@@H]21 NVEQFIOZRFFVFW-RGCMKSIDSA-N 0.000 description 3
MMFCJPPRCYDLLZ-UHFFFAOYSA-N dec-2-enal Chemical compound CCCCCCCC=CC=O MMFCJPPRCYDLLZ-UHFFFAOYSA-N 0.000 description 3
238000001514 detection method Methods 0.000 description 3
AZOCECCLWFDTAP-UHFFFAOYSA-N dihydrocarvone Chemical compound CC1CCC(C(C)=C)CC1=O AZOCECCLWFDTAP-UHFFFAOYSA-N 0.000 description 3
235000013870 dimethyl polysiloxane Nutrition 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
238000001035 drying Methods 0.000 description 3
238000004945 emulsification Methods 0.000 description 3
238000007720 emulsion polymerization reaction Methods 0.000 description 3
239000012530 fluid Substances 0.000 description 3
125000000524 functional group Chemical group 0.000 description 3
150000002314 glycerols Chemical class 0.000 description 3
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 3
125000005842 heteroatom Chemical group 0.000 description 3
125000001183 hydrocarbyl group Chemical group 0.000 description 3
150000002466 imines Chemical class 0.000 description 3
239000003999 initiator Substances 0.000 description 3
150000002500 ions Chemical class 0.000 description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
ZYTMANIQRDEHIO-KXUCPTDWSA-N isopulegol Chemical compound C[C@@H]1CC[C@@H](C(C)=C)[C@H](O)C1 ZYTMANIQRDEHIO-KXUCPTDWSA-N 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
KVWWIYGFBYDJQC-UHFFFAOYSA-N methyl dihydrojasmonate Chemical compound CCCCCC1C(CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-UHFFFAOYSA-N 0.000 description 3
BNWJOHGLIBDBOB-UHFFFAOYSA-N myristicin Chemical compound COC1=CC(CC=C)=CC2=C1OCO2 BNWJOHGLIBDBOB-UHFFFAOYSA-N 0.000 description 3
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 3
WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 3
235000021313 oleic acid Nutrition 0.000 description 3
150000002924 oxiranes Chemical class 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
239000002245 particle Substances 0.000 description 3
229910052698 phosphorus Inorganic materials 0.000 description 3
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
238000012545 processing Methods 0.000 description 3
239000002964 rayon Substances 0.000 description 3
ZMQAAUBTXCXRIC-UHFFFAOYSA-N safrole Chemical compound C=CCC1=CC=C2OCOC2=C1 ZMQAAUBTXCXRIC-UHFFFAOYSA-N 0.000 description 3
230000001953 sensory effect Effects 0.000 description 3
230000035943 smell Effects 0.000 description 3
239000008107 starch Substances 0.000 description 3
XJPBRODHZKDRCB-UHFFFAOYSA-N trans-alpha-ocimene Natural products CC(=C)CCC=C(C)C=C XJPBRODHZKDRCB-UHFFFAOYSA-N 0.000 description 3
BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 3
XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
235000015112 vegetable and seed oil Nutrition 0.000 description 3
IHPKGUQCSIINRJ-UHFFFAOYSA-N β-ocimene Natural products CC(C)=CCC=C(C)C=C IHPKGUQCSIINRJ-UHFFFAOYSA-N 0.000 description 3
KRCZYMFUWVJCLI-GUBZILKMSA-N (+)-dihydrocarveol Chemical compound C[C@H]1CC[C@H](C(C)=C)C[C@@H]1O KRCZYMFUWVJCLI-GUBZILKMSA-N 0.000 description 2
GRWFGVWFFZKLTI-RKDXNWHRSA-N (+)-α-pinene Chemical compound CC1=CC[C@H]2C(C)(C)[C@@H]1C2 GRWFGVWFFZKLTI-RKDXNWHRSA-N 0.000 description 2
QMVPMAAFGQKVCJ-JTQLQIEISA-N (-)-Citronellol Chemical compound OCC[C@@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-JTQLQIEISA-N 0.000 description 2
RGZSQWQPBWRIAQ-CABCVRRESA-N (-)-alpha-Bisabolol Chemical compound CC(C)=CCC[C@](C)(O)[C@H]1CCC(C)=CC1 RGZSQWQPBWRIAQ-CABCVRRESA-N 0.000 description 2
LKKDASYGWYYFIK-UHFFFAOYSA-N (-)-cryptomeridiol Natural products C1CCC(C)(O)C2CC(C(C)(O)C)CCC21C LKKDASYGWYYFIK-UHFFFAOYSA-N 0.000 description 2
KXSDPILWMGFJMM-AEJSXWLSSA-N (1s,4r,5r)-4-methyl-1-propan-2-ylbicyclo[3.1.0]hexan-4-ol Chemical compound C([C@]1(O)C)C[C@]2(C(C)C)[C@H]1C2 KXSDPILWMGFJMM-AEJSXWLSSA-N 0.000 description 2
XRZFVPCFHPIMAD-UHFFFAOYSA-N (2-ethoxy-4-formylphenyl) acetate Chemical compound CCOC1=CC(C=O)=CC=C1OC(C)=O XRZFVPCFHPIMAD-UHFFFAOYSA-N 0.000 description 2
HPZWSJQQCJZBBG-LQPGMRSMSA-N (3E,5E)-2,6-Dimethyl-1,3,5,7-octatetraene Chemical compound CC(=C)\C=C\C=C(/C)C=C HPZWSJQQCJZBBG-LQPGMRSMSA-N 0.000 description 2
125000006702 (C1-C18) alkyl group Chemical group 0.000 description 2
TYDDWHVJHGIJCW-UHFFFAOYSA-N (E)-2,6-dimethyl-octa-1,5,7-trien-3-ol Natural products CC(=C)C(O)CC=C(C)C=C TYDDWHVJHGIJCW-UHFFFAOYSA-N 0.000 description 2
OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 2
SSNZFFBDIMUILS-ZHACJKMWSA-N (E)-dodec-2-enal Chemical compound CCCCCCCCC\C=C\C=O SSNZFFBDIMUILS-ZHACJKMWSA-N 0.000 description 2
QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 2
XJHRZBIBSSVCEL-ARJAWSKDSA-N (Z)-non-6-en-1-ol Chemical compound CC\C=C/CCCCCO XJHRZBIBSSVCEL-ARJAWSKDSA-N 0.000 description 2
LDUYDLGCMTVIIO-VOTSOKGWSA-N (e)-1-(1-methoxypropoxy)hex-3-ene Chemical compound CC\C=C\CCOC(CC)OC LDUYDLGCMTVIIO-VOTSOKGWSA-N 0.000 description 2
ZCHHRLHTBGRGOT-PLNGDYQASA-N (z)-hex-2-en-1-ol Chemical compound CCC\C=C/CO ZCHHRLHTBGRGOT-PLNGDYQASA-N 0.000 description 2
RFFOTVCVTJUTAD-AOOOYVTPSA-N 1,4-cineole Chemical compound CC(C)[C@]12CC[C@](C)(CC1)O2 RFFOTVCVTJUTAD-AOOOYVTPSA-N 0.000 description 2
MPCAJMNYNOGXPB-SLPGGIOYSA-N 1,5-anhydro-D-glucitol Chemical class OC[C@H]1OC[C@H](O)[C@@H](O)[C@@H]1O MPCAJMNYNOGXPB-SLPGGIOYSA-N 0.000 description 2
VNQXSTWCDUXYEZ-UHFFFAOYSA-N 1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione Chemical compound C1CC2(C)C(=O)C(=O)C1C2(C)C VNQXSTWCDUXYEZ-UHFFFAOYSA-N 0.000 description 2
MISTZQJSHHTDCF-UHFFFAOYSA-N 1-(1-propoxyethoxy)propane Chemical compound CCCOC(C)OCCC MISTZQJSHHTDCF-UHFFFAOYSA-N 0.000 description 2
LMWNGLDCJDIIBR-CMDGGOBGSA-N 1-(2,6,6-Trimethyl-1-cyclohexen-1-yl)-1-penten-3-one Chemical compound CCC(=O)\C=C\C1=C(C)CCCC1(C)C LMWNGLDCJDIIBR-CMDGGOBGSA-N 0.000 description 2
CRIGTVCBMUKRSL-FNORWQNLSA-N 1-(2,6,6-trimethylcyclohex-2-en-1-yl)but-2-enone Chemical compound C\C=C\C(=O)C1C(C)=CCCC1(C)C CRIGTVCBMUKRSL-FNORWQNLSA-N 0.000 description 2
XDFCZUMLNOYOCH-UHFFFAOYSA-N 1-hydroxydecan-3-one Chemical compound CCCCCCCC(=O)CCO XDFCZUMLNOYOCH-UHFFFAOYSA-N 0.000 description 2
KYGSYTRHCDNSGS-UHFFFAOYSA-N 1-phenylpent-4-en-1-one Chemical compound C=CCCC(=O)C1=CC=CC=C1 KYGSYTRHCDNSGS-UHFFFAOYSA-N 0.000 description 2
ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 2
QEHNNAQSHBJMTJ-UHFFFAOYSA-N 2,2,3,3,4,4-hexamethyl-1h-naphthalene Chemical compound C1=CC=C2C(C)(C)C(C)(C)C(C)(C)CC2=C1 QEHNNAQSHBJMTJ-UHFFFAOYSA-N 0.000 description 2
LIMXJCIGROLRED-SOFGYWHQSA-N 2,2-dimethyl-3-[(2e)-3-methylpenta-2,4-dienyl]oxirane Chemical compound C=CC(/C)=C/CC1OC1(C)C LIMXJCIGROLRED-SOFGYWHQSA-N 0.000 description 2
UCTUXUGXIFRVGX-UHFFFAOYSA-N 2,3,4-trimethoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C(OC)=C1OC UCTUXUGXIFRVGX-UHFFFAOYSA-N 0.000 description 2
IAJBQAYHSQIQRE-UHFFFAOYSA-N 2,4,5-trimethoxybenzaldehyde Chemical compound COC1=CC(OC)=C(C=O)C=C1OC IAJBQAYHSQIQRE-UHFFFAOYSA-N 0.000 description 2
ZHHYXNZJDGDGPJ-UHFFFAOYSA-N 2,4-Nonadienal Natural products CCCCC=CC=CC=O ZHHYXNZJDGDGPJ-UHFFFAOYSA-N 0.000 description 2
FAMPSKZZVDUYOS-UHFFFAOYSA-N 2,6,6,9-tetramethylcycloundeca-1,4,8-triene Chemical compound CC1=CCC(C)(C)C=CCC(C)=CCC1 FAMPSKZZVDUYOS-UHFFFAOYSA-N 0.000 description 2
KWHVBVJDKLSOTB-UHFFFAOYSA-N 2-(3-methylphenyl)ethanol Chemical compound CC1=CC=CC(CCO)=C1 KWHVBVJDKLSOTB-UHFFFAOYSA-N 0.000 description 2
VMLYBYNXKMHLIJ-UHFFFAOYSA-N 2-(4-tert-butylphenyl)acetaldehyde Chemical compound CC(C)(C)C1=CC=C(CC=O)C=C1 VMLYBYNXKMHLIJ-UHFFFAOYSA-N 0.000 description 2
AWNOGHRWORTNEI-UHFFFAOYSA-N 2-(6,6-dimethyl-4-bicyclo[3.1.1]hept-3-enyl)ethyl acetate Chemical compound CC(=O)OCCC1=CCC2C(C)(C)C1C2 AWNOGHRWORTNEI-UHFFFAOYSA-N 0.000 description 2
HVGZQCSMLUDISR-UHFFFAOYSA-N 2-Phenylethyl propanoate Chemical compound CCC(=O)OCCC1=CC=CC=C1 HVGZQCSMLUDISR-UHFFFAOYSA-N 0.000 description 2
UFOUDYPOSJJEDJ-UHFFFAOYSA-N 2-Phenylpropionaldehyde dimethyl acetal Chemical compound COC(OC)C(C)C1=CC=CC=C1 UFOUDYPOSJJEDJ-UHFFFAOYSA-N 0.000 description 2
PUAQLLVFLMYYJJ-UHFFFAOYSA-N 2-aminopropiophenone Chemical compound CC(N)C(=O)C1=CC=CC=C1 PUAQLLVFLMYYJJ-UHFFFAOYSA-N 0.000 description 2
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
QTJISTOHDJAKOQ-UHFFFAOYSA-N 2-hydroxyethylazanium;methyl sulfate Chemical compound [NH3+]CCO.COS([O-])(=O)=O QTJISTOHDJAKOQ-UHFFFAOYSA-N 0.000 description 2
OFLXNHNYPQPQKW-UHFFFAOYSA-N 2-isopropyl-4-methylthiazole Chemical compound CC(C)C1=NC(C)=CS1 OFLXNHNYPQPQKW-UHFFFAOYSA-N 0.000 description 2
RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical compound CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 description 2
LBLYYCQCTBFVLH-UHFFFAOYSA-M 2-methylbenzenesulfonate Chemical compound CC1=CC=CC=C1S([O-])(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-M 0.000 description 2
HSINXSRFDIJUQN-UHFFFAOYSA-N 2-methylidenebicyclo[7.2.0]undecane Chemical compound C=C1CCCCCCC2CCC12 HSINXSRFDIJUQN-UHFFFAOYSA-N 0.000 description 2
IKDIJXDZEYHZSD-UHFFFAOYSA-N 2-phenylethyl formate Chemical compound O=COCCC1=CC=CC=C1 IKDIJXDZEYHZSD-UHFFFAOYSA-N 0.000 description 2
DGKXDLCVQSQVBC-UHFFFAOYSA-N 3,5,5-trimethylhexyl acetate Chemical compound CC(C)(C)CC(C)CCOC(C)=O DGKXDLCVQSQVBC-UHFFFAOYSA-N 0.000 description 2
MAGDHSMUSSJMGW-UHFFFAOYSA-N 3-(1h-inden-5-yl)propanal Chemical compound O=CCCC1=CC=C2CC=CC2=C1 MAGDHSMUSSJMGW-UHFFFAOYSA-N 0.000 description 2
VAJVDSVGBWFCLW-UHFFFAOYSA-N 3-Phenyl-1-propanol Chemical compound OCCCC1=CC=CC=C1 VAJVDSVGBWFCLW-UHFFFAOYSA-N 0.000 description 2
BXGDBHAMTMMNTO-UHFFFAOYSA-N 3-azaniumyl-3-(4-chlorophenyl)propanoate Chemical compound OC(=O)CC(N)C1=CC=C(Cl)C=C1 BXGDBHAMTMMNTO-UHFFFAOYSA-N 0.000 description 2
LULAYUGMBFYYEX-UHFFFAOYSA-N 3-chlorobenzoic acid Chemical compound OC(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-N 0.000 description 2
MFKRHJVUCZRDTF-UHFFFAOYSA-N 3-methoxy-3-methylbutan-1-ol Chemical compound COC(C)(C)CCO MFKRHJVUCZRDTF-UHFFFAOYSA-N 0.000 description 2
HFNGYHHRRMSKEU-UHFFFAOYSA-N 4-Methoxybenzyl acetate Chemical compound COC1=CC=C(COC(C)=O)C=C1 HFNGYHHRRMSKEU-UHFFFAOYSA-N 0.000 description 2
XPDORSROGAZEGY-UHFFFAOYSA-N 4-Methoxybenzyl formate Chemical compound COC1=CC=C(COC=O)C=C1 XPDORSROGAZEGY-UHFFFAOYSA-N 0.000 description 2
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical group OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
XQXPVVBIMDBYFF-UHFFFAOYSA-N 4-hydroxyphenylacetic acid Chemical compound OC(=O)CC1=CC=C(O)C=C1 XQXPVVBIMDBYFF-UHFFFAOYSA-N 0.000 description 2
JJWWUTCHOAKZPR-UHFFFAOYSA-N 4-methylpent-4-en-2-yl 2-methylpropanoate Chemical compound CC(C)C(=O)OC(C)CC(C)=C JJWWUTCHOAKZPR-UHFFFAOYSA-N 0.000 description 2
GDWRKZLROIFUML-UHFFFAOYSA-N 4-phenylbutan-2-ol Chemical compound CC(O)CCC1=CC=CC=C1 GDWRKZLROIFUML-UHFFFAOYSA-N 0.000 description 2
IZBHWLYKWKYMOY-UHFFFAOYSA-N 5-chloro-6-methoxypyridine-3-carbaldehyde Chemical compound COC1=NC=C(C=O)C=C1Cl IZBHWLYKWKYMOY-UHFFFAOYSA-N 0.000 description 2
BGEBZHIAGXMEMV-UHFFFAOYSA-N 5-methoxypsoralen Chemical compound O1C(=O)C=CC2=C1C=C1OC=CC1=C2OC BGEBZHIAGXMEMV-UHFFFAOYSA-N 0.000 description 2
XTXZCNATVCIKTR-UHFFFAOYSA-N 5-methyl-4-phenyl-1h-pyrazole Chemical compound N1N=CC(C=2C=CC=CC=2)=C1C XTXZCNATVCIKTR-UHFFFAOYSA-N 0.000 description 2
PSBKJPTZCVYXSD-UHFFFAOYSA-N 5-methylheptan-3-one Chemical compound CCC(C)CC(=O)CC PSBKJPTZCVYXSD-UHFFFAOYSA-N 0.000 description 2
OUXAABAEPHHZPC-UHFFFAOYSA-N 6,6-dimethylspiro[bicyclo[3.1.1]heptane-4,2'-oxirane] Chemical compound CC1(C)C(CC2)CC1C12CO1 OUXAABAEPHHZPC-UHFFFAOYSA-N 0.000 description 2
UCQHFDKBUHCAFR-ILXRZTDVSA-N 7-epi-sesquithujene Chemical compound CC1=CC[C@]2([C@@H](CCC=C(C)C)C)[C@H]1C2 UCQHFDKBUHCAFR-ILXRZTDVSA-N 0.000 description 2
IDWULKZGRNHZNR-UHFFFAOYSA-N 7-methoxy-3,7-dimethyloctanal Chemical compound COC(C)(C)CCCC(C)CC=O IDWULKZGRNHZNR-UHFFFAOYSA-N 0.000 description 2
QDTDKYHPHANITQ-UHFFFAOYSA-N 7-methyloctan-1-ol Chemical compound CC(C)CCCCCCO QDTDKYHPHANITQ-UHFFFAOYSA-N 0.000 description 2
ROWKJAVDOGWPAT-UHFFFAOYSA-N Acetoin Chemical compound CC(O)C(C)=O ROWKJAVDOGWPAT-UHFFFAOYSA-N 0.000 description 2
ITYNGVSTWVVPIC-XGFWRYKXSA-N Alloaromadendrene Natural products C([C@@H]1[C@H]2C1(C)C)CC(=C)[C@@H]1[C@@H]2[C@H](C)CC1 ITYNGVSTWVVPIC-XGFWRYKXSA-N 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
235000019737 Animal fat Nutrition 0.000 description 2
240000002791 Brassica napus Species 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
KVUKSYNHMWOWOJ-UHFFFAOYSA-N C=C1C2CCCC(CCC1)C2 Chemical compound C=C1C2CCCC(CCC1)C2 KVUKSYNHMWOWOJ-UHFFFAOYSA-N 0.000 description 2
CCEFMUBVSUDRLG-KXUCPTDWSA-N D-limonene 1,2-Epoxide Chemical compound C1[C@H](C(=C)C)CC[C@@]2(C)O[C@H]21 CCEFMUBVSUDRLG-KXUCPTDWSA-N 0.000 description 2
JHJCHCSUEGPIGE-UHFFFAOYSA-N Dihydro-alpha-ionone Natural products CC(=O)CCC1C(C)=CCCC1(C)C JHJCHCSUEGPIGE-UHFFFAOYSA-N 0.000 description 2
TUSIZTVSUSBSQI-UHFFFAOYSA-N Dihydrocarveol acetate Chemical compound CC1CCC(C(C)=C)CC1OC(C)=O TUSIZTVSUSBSQI-UHFFFAOYSA-N 0.000 description 2
241000196324 Embryophyta Species 0.000 description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
GOMAKLPNAAZVCJ-UHFFFAOYSA-N Ethyl phenylglycidate Chemical compound CCOC(=O)C1OC1C1=CC=CC=C1 GOMAKLPNAAZVCJ-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
WEEGYLXZBRQIMU-WAAGHKOSSA-N Eucalyptol Chemical compound C1C[C@H]2CC[C@]1(C)OC2(C)C WEEGYLXZBRQIMU-WAAGHKOSSA-N 0.000 description 2
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
PDEQKAVEYSOLJX-UHFFFAOYSA-N Hexahydronerolidol Natural products C1C2C3(C)C2CC1C3(C)CCC=C(CO)C PDEQKAVEYSOLJX-UHFFFAOYSA-N 0.000 description 2
MZNHUHNWGVUEAT-XBXARRHUSA-N Hexyl crotonate Chemical compound CCCCCCOC(=O)\C=C\C MZNHUHNWGVUEAT-XBXARRHUSA-N 0.000 description 2
QILMAYXCYBTEDM-IWQZZHSRSA-N Isoambrettolide Chemical compound O=C1CCCCCCC\C=C/CCCCCCO1 QILMAYXCYBTEDM-IWQZZHSRSA-N 0.000 description 2
HICAMHOOTMOHPA-UHFFFAOYSA-N Isofuranogermacren Natural products C1C(C=C)(C)C(C(=C)C)CC2=C1OC=C2C HICAMHOOTMOHPA-UHFFFAOYSA-N 0.000 description 2
RNKZFOIQKCQOAQ-UHFFFAOYSA-N Isopimpinellin Natural products COC1CC(=O)Oc2c(OC)c3occc3cc12 RNKZFOIQKCQOAQ-UHFFFAOYSA-N 0.000 description 2
BVQAARKEKMVAKI-UHFFFAOYSA-N Khusimol Natural products CC1(C)C2CCC(=C)C3CCC(CO)C13C2 BVQAARKEKMVAKI-UHFFFAOYSA-N 0.000 description 2
MQWIFDHBNGIVPO-UHFFFAOYSA-N Kusunol Natural products C1CC(C(C)(C)O)CC2(C)C(C)CCC=C21 MQWIFDHBNGIVPO-UHFFFAOYSA-N 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 2
239000005639 Lauric acid Substances 0.000 description 2
235000021353 Lignoceric acid Nutrition 0.000 description 2
CQXMAMUUWHYSIY-UHFFFAOYSA-N Lignoceric acid Natural products CCCCCCCCCCCCCCCCCCCCCCCC(=O)OCCC1=CC=C(O)C=C1 CQXMAMUUWHYSIY-UHFFFAOYSA-N 0.000 description 2
BRHDDEIRQPDPMG-UHFFFAOYSA-N Linalyl oxide Chemical compound CC(C)(O)C1CCC(C)(C=C)O1 BRHDDEIRQPDPMG-UHFFFAOYSA-N 0.000 description 2
LAEIZWJAQRGPDA-UHFFFAOYSA-N Manoyloxid Natural products CC1(C)CCCC2(C)C3CC=C(C)OC3(C)CCC21 LAEIZWJAQRGPDA-UHFFFAOYSA-N 0.000 description 2
229920000877 Melamine resin Polymers 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
IJFKZRMIRAVXRK-UHFFFAOYSA-N Ocimenol Natural products C=CC(C)=CCCC(C)(C)O IJFKZRMIRAVXRK-UHFFFAOYSA-N 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
235000019482 Palm oil Nutrition 0.000 description 2
GGHMUJBZYLPWFD-MYYUVRNCSA-N Patchouli alcohol Natural products O[C@@]12C(C)(C)[C@H]3C[C@H]([C@H](C)CC1)[C@]2(C)CC3 GGHMUJBZYLPWFD-MYYUVRNCSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
UIKJRDSCEYGECG-UHFFFAOYSA-N Phenylmethyl 2-methylpropanoate Chemical compound CC(C)C(=O)OCC1=CC=CC=C1 UIKJRDSCEYGECG-UHFFFAOYSA-N 0.000 description 2
VONGZNXBKCOUHB-UHFFFAOYSA-N Phenylmethyl butanoate Chemical compound CCCC(=O)OCC1=CC=CC=C1 VONGZNXBKCOUHB-UHFFFAOYSA-N 0.000 description 2
LQKRYVGRPXFFAV-UHFFFAOYSA-N Phenylmethylglycidic ester Chemical compound CCOC(=O)C1OC1(C)C1=CC=CC=C1 LQKRYVGRPXFFAV-UHFFFAOYSA-N 0.000 description 2
KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
239000002262 Schiff base Substances 0.000 description 2
IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 2
KMJLGCYDCCCRHH-UHFFFAOYSA-N Spathulenol Natural products CC1(O)CCC2(C)C1C3C(CCC2=C)C3(C)C KMJLGCYDCCCRHH-UHFFFAOYSA-N 0.000 description 2
DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 description 2
BGKAKRUFBSTALK-UHFFFAOYSA-N Vanillin isobutyrate Chemical compound COC1=CC(C=O)=CC=C1OC(=O)C(C)C BGKAKRUFBSTALK-UHFFFAOYSA-N 0.000 description 2
SPJRLGBKRAHBQE-UHFFFAOYSA-N [3-[(2-chloro-2-methylpentanoyl)amino]phenyl] n-methylcarbamate Chemical compound CCCC(C)(Cl)C(=O)NC1=CC=CC(OC(=O)NC)=C1 SPJRLGBKRAHBQE-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
239000004480 active ingredient Substances 0.000 description 2
125000002015 acyclic group Chemical group 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
150000001299 aldehydes Chemical class 0.000 description 2
PYMYPHUHKUWMLA-VPENINKCSA-N aldehydo-D-xylose Chemical compound OC[C@@H](O)[C@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-VPENINKCSA-N 0.000 description 2
125000003282 alkyl amino group Chemical group 0.000 description 2
125000005376 alkyl siloxane group Chemical group 0.000 description 2
PDEQKAVEYSOLJX-AIEDFZFUSA-N alpha-Santalol Natural products CC(=CCC[C@@]1(C)[C@H]2C[C@@H]3[C@H](C2)[C@]13C)CO PDEQKAVEYSOLJX-AIEDFZFUSA-N 0.000 description 2
PFSTYGCNVAVZBK-JQGMZEBDSA-N alpha-Sinensal Chemical compound O=CC(/C)=C/CCC(/C)=C/C\C=C(/C)C=C PFSTYGCNVAVZBK-JQGMZEBDSA-N 0.000 description 2
QMAYBMKBYCGXDH-UHFFFAOYSA-N alpha-amorphene Natural products C1CC(C)=CC2C(C(C)C)CC=C(C)C21 QMAYBMKBYCGXDH-UHFFFAOYSA-N 0.000 description 2
YHBUQBJHSRGZNF-HNNXBMFYSA-N alpha-bisabolene Natural products CC(C)=CCC=C(C)[C@@H]1CCC(C)=CC1 YHBUQBJHSRGZNF-HNNXBMFYSA-N 0.000 description 2
QMAYBMKBYCGXDH-KKUMJFAQSA-N alpha-cadinene Chemical compound C1CC(C)=C[C@H]2[C@H](C(C)C)CC=C(C)[C@@H]21 QMAYBMKBYCGXDH-KKUMJFAQSA-N 0.000 description 2
IPZIYGAXCZTOMH-UHFFFAOYSA-N alpha-eudesmol Natural products CC1=CCCC2CCC(CC12)C(C)(C)O IPZIYGAXCZTOMH-UHFFFAOYSA-N 0.000 description 2
ADIDQIZBYUABQK-RWMBFGLXSA-N alpha-guaiene Chemical compound C1([C@H](CC[C@H](C2)C(C)=C)C)=C2[C@@H](C)CC1 ADIDQIZBYUABQK-RWMBFGLXSA-N 0.000 description 2
FJNHFUOCVLERHW-UHFFFAOYSA-N alpha-gurjunene Natural products CC1CCC2C(C3=CCCC13)C2(C)C FJNHFUOCVLERHW-UHFFFAOYSA-N 0.000 description 2
ZJSIKVDEOWWVEH-UHFFFAOYSA-N alpha-himachalene Chemical compound C=C1CCCC(C)(C)C2C1CCC(C)=C2 ZJSIKVDEOWWVEH-UHFFFAOYSA-N 0.000 description 2
QUMXDOLUJCHOAY-UHFFFAOYSA-N alpha-methylbenzyl acetate Natural products CC(=O)OC(C)C1=CC=CC=C1 QUMXDOLUJCHOAY-UHFFFAOYSA-N 0.000 description 2
OZQAPQSEYFAMCY-UHFFFAOYSA-N alpha-selinene Natural products C1CC=C(C)C2CC(C(=C)C)CCC21C OZQAPQSEYFAMCY-UHFFFAOYSA-N 0.000 description 2
NIIPDXITZPFFTE-NHYWBVRUSA-N alpha-vetivone Natural products O=C1C=C2[C@](C)([C@@H](C)C1)C/C(=C(/C)\C)/CC2 NIIPDXITZPFFTE-NHYWBVRUSA-N 0.000 description 2
LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
229940011037 anethole Drugs 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
NGHOLYJTSCBCGC-VAWYXSNFSA-N benzyl cinnamate Chemical compound C=1C=CC=CC=1/C=C/C(=O)OCC1=CC=CC=C1 NGHOLYJTSCBCGC-VAWYXSNFSA-N 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
DYLPEFGBWGEFBB-UHFFFAOYSA-N beta-Cedren Natural products C1C23C(C)CCC3C(C)(C)C1C(=C)CC2 DYLPEFGBWGEFBB-UHFFFAOYSA-N 0.000 description 2
NOPLRNXKHZRXHT-YFVJMOTDSA-N beta-Sinensal Chemical compound O=CC(/C)=C/CCC(/C)=C/CCC(=C)C=C NOPLRNXKHZRXHT-YFVJMOTDSA-N 0.000 description 2
UPVZPMJSRSWJHQ-UHFFFAOYSA-N beta-Ylangen Natural products C1CC(=C)C2C3(C)CCC(C(C)C)C2C31 UPVZPMJSRSWJHQ-UHFFFAOYSA-N 0.000 description 2
JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 2
ISLOGSAEQNKPGG-DOMZBBRYSA-N beta-vetivone Natural products C[C@@H]1CC(=O)C=C(C)[C@]11CC(=C(C)C)CC1 ISLOGSAEQNKPGG-DOMZBBRYSA-N 0.000 description 2
239000000828 canola oil Substances 0.000 description 2
235000019519 canola oil Nutrition 0.000 description 2
150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
239000003093 cationic surfactant Substances 0.000 description 2
229940026455 cedrol Drugs 0.000 description 2
PCROEXHGMUJCDB-UHFFFAOYSA-N cedrol Natural products CC1CCC2C(C)(C)C3CC(C)(O)CC12C3 PCROEXHGMUJCDB-UHFFFAOYSA-N 0.000 description 2
AHZYNUWTBDLJHG-RHBQXOTJSA-N cedryl formate Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1[C@@](OC=O)(C)CC2 AHZYNUWTBDLJHG-RHBQXOTJSA-N 0.000 description 2
FLKYBGKDCCEQQM-WYUVZMMLSA-M cefazolin sodium Chemical compound [Na+].S1C(C)=NN=C1SCC1=C(C([O-])=O)N2C(=O)[C@@H](NC(=O)CN3N=NN=C3)[C@H]2SC1 FLKYBGKDCCEQQM-WYUVZMMLSA-M 0.000 description 2
HQKQRXZEXPXXIG-VJOHVRBBSA-N chembl2333940 Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@H]1[C@@](OC(C)=O)(C)CC2 HQKQRXZEXPXXIG-VJOHVRBBSA-N 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
238000000576 coating method Methods 0.000 description 2
MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 description 2
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 2
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 2
239000003599 detergent Substances 0.000 description 2
238000011161 development Methods 0.000 description 2
AQIXEPGDORPWBJ-UHFFFAOYSA-N diethyl carbinol Natural products CCC(O)CC AQIXEPGDORPWBJ-UHFFFAOYSA-N 0.000 description 2
GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
239000004205 dimethyl polysiloxane Substances 0.000 description 2
150000002016 disaccharides Chemical class 0.000 description 2
WTOYNNBCKUYIKC-UHFFFAOYSA-N dl-nootkatone Natural products C1CC(C(C)=C)CC2(C)C(C)CC(=O)C=C21 WTOYNNBCKUYIKC-UHFFFAOYSA-N 0.000 description 2
239000003623 enhancer Substances 0.000 description 2
230000032050 esterification Effects 0.000 description 2
238000000605 extraction Methods 0.000 description 2
239000003925 fat Substances 0.000 description 2
235000019197 fats Nutrition 0.000 description 2
150000002190 fatty acyls Chemical group 0.000 description 2
IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 2
DUYRYUZIBGFLDD-UHFFFAOYSA-N gamma-gurjunene Chemical compound CC1CCC(C(C)=C)C=C2C(C)CCC21 DUYRYUZIBGFLDD-UHFFFAOYSA-N 0.000 description 2
238000007429 general method Methods 0.000 description 2
FQMZVFJYMPNUCT-UHFFFAOYSA-N geraniol formate Natural products CC(C)=CCCC(C)=CCOC=O FQMZVFJYMPNUCT-UHFFFAOYSA-N 0.000 description 2
GXEGJTGWYVZSNR-OMQMMEOVSA-N germacrene-B Natural products CC(C)=C1CC\C(C)=C/CC\C(C)=C/C1 GXEGJTGWYVZSNR-OMQMMEOVSA-N 0.000 description 2
FXHGMKSSBGDXIY-UHFFFAOYSA-N heptanal Chemical compound CCCCCCC=O FXHGMKSSBGDXIY-UHFFFAOYSA-N 0.000 description 2
LIIALPBMIOVAHH-UHFFFAOYSA-N herniarin Chemical compound C1=CC(=O)OC2=CC(OC)=CC=C21 LIIALPBMIOVAHH-UHFFFAOYSA-N 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
JTCIUOKKVACNCK-BJMVGYQFSA-N hexyl (e)-2-methylbut-2-enoate Chemical compound CCCCCCOC(=O)C(\C)=C\C JTCIUOKKVACNCK-BJMVGYQFSA-N 0.000 description 2
125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
125000004356 hydroxy functional group Chemical group O* 0.000 description 2
239000012535 impurity Substances 0.000 description 2
PQNFLJBBNBOBRQ-UHFFFAOYSA-N indane Chemical compound C1=CC=C2CCCC2=C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 description 2
PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 2
RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 2
VFTGLSWXJMRZNB-UHFFFAOYSA-N isoamyl isobutyrate Chemical compound CC(C)CCOC(=O)C(C)C VFTGLSWXJMRZNB-UHFFFAOYSA-N 0.000 description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
IUSBVFZKQJGVEP-SNAWJCMRSA-N isoeugenol acetate Chemical compound COC1=CC(\C=C\C)=CC=C1OC(C)=O IUSBVFZKQJGVEP-SNAWJCMRSA-N 0.000 description 2
NFLGAXVYCFJBMK-UHFFFAOYSA-N isomenthone Natural products CC(C)C1CCC(C)CC1=O NFLGAXVYCFJBMK-UHFFFAOYSA-N 0.000 description 2
SVURIXNDRWRAFU-UHFFFAOYSA-N juniperanol Natural products C1C23C(C)CCC3C(C)(C)C1C(O)(C)CC2 SVURIXNDRWRAFU-UHFFFAOYSA-N 0.000 description 2
239000000944 linseed oil Substances 0.000 description 2
235000021388 linseed oil Nutrition 0.000 description 2
239000007788 liquid Substances 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
KVWWIYGFBYDJQC-QWRGUYRKSA-N methyl 2-[(1s,2s)-3-oxo-2-pentylcyclopentyl]acetate Chemical compound CCCCC[C@H]1[C@H](CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-QWRGUYRKSA-N 0.000 description 2
BFBPISPWJZMWJN-UHFFFAOYSA-N methyl 2-[(7-hydroxy-3,7-dimethyloctylidene)amino]benzoate Chemical compound COC(=O)C1=CC=CC=C1N=CCC(C)CCCC(C)(C)O BFBPISPWJZMWJN-UHFFFAOYSA-N 0.000 description 2
IPWBXORAIBJDDQ-UHFFFAOYSA-N methyl 2-hexyl-3-oxocyclopentane-1-carboxylate Chemical compound CCCCCCC1C(C(=O)OC)CCC1=O IPWBXORAIBJDDQ-UHFFFAOYSA-N 0.000 description 2
CUUJGDIRLBSKGU-UHFFFAOYSA-N methyl hydrogen sulfate;propan-1-amine Chemical compound CCC[NH3+].COS([O-])(=O)=O CUUJGDIRLBSKGU-UHFFFAOYSA-N 0.000 description 2
CCRCUPLGCSFEDV-BQYQJAHWSA-N methyl trans-cinnamate Chemical compound COC(=O)\C=C\C1=CC=CC=C1 CCRCUPLGCSFEDV-BQYQJAHWSA-N 0.000 description 2
238000002156 mixing Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
239000003608 nonionic fabric softener Substances 0.000 description 2
239000004669 nonionic softener Substances 0.000 description 2
239000004745 nonwoven fabric Substances 0.000 description 2
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
125000006353 oxyethylene group Chemical group 0.000 description 2
UPPSFGGDKACIKP-UHFFFAOYSA-N p-Tolyl isobutyrate Chemical compound CC(C)C(=O)OC1=CC=C(C)C=C1 UPPSFGGDKACIKP-UHFFFAOYSA-N 0.000 description 2
239000002540 palm oil Substances 0.000 description 2
230000036961 partial effect Effects 0.000 description 2
ISBHMJZRKAFTGE-UHFFFAOYSA-N pent-2-enenitrile Chemical compound CCC=CC#N ISBHMJZRKAFTGE-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
239000010452 phosphate Substances 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
LCYXQUJDODZYIJ-UHFFFAOYSA-N pinocarveol Chemical compound C1C2C(C)(C)C1CC(O)C2=C LCYXQUJDODZYIJ-UHFFFAOYSA-N 0.000 description 2
229920000570 polyether Polymers 0.000 description 2
229920005862 polyol Polymers 0.000 description 2
150000003077 polyols Chemical class 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000002243 precursor Substances 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
125000001453 quaternary ammonium group Chemical group 0.000 description 2
239000002994 raw material Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
230000002829 reductive effect Effects 0.000 description 2
235000003441 saturated fatty acids Nutrition 0.000 description 2
150000004671 saturated fatty acids Chemical class 0.000 description 2
HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 2
ZFRKQXVRDFCRJG-UHFFFAOYSA-N skatole Chemical compound C1=CC=C2C(C)=CNC2=C1 ZFRKQXVRDFCRJG-UHFFFAOYSA-N 0.000 description 2
239000001587 sorbitan monostearate Substances 0.000 description 2
235000011076 sorbitan monostearate Nutrition 0.000 description 2
229940035048 sorbitan monostearate Drugs 0.000 description 2
235000012424 soybean oil Nutrition 0.000 description 2
239000003549 soybean oil Substances 0.000 description 2
241000894007 species Species 0.000 description 2
238000000547 structure data Methods 0.000 description 2
150000005846 sugar alcohols Polymers 0.000 description 2
239000000375 suspending agent Substances 0.000 description 2
QJVXKWHHAMZTBY-GCPOEHJPSA-N syringin Chemical compound COC1=CC(\C=C\CO)=CC(OC)=C1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 QJVXKWHHAMZTBY-GCPOEHJPSA-N 0.000 description 2
LHYHMMRYTDARSZ-YJNKXOJESA-N t-cadinol Natural products C1CC(C)=C[C@@H]2[C@H](C(C)C)CC[C@](C)(O)[C@@H]21 LHYHMMRYTDARSZ-YJNKXOJESA-N 0.000 description 2
LHYHMMRYTDARSZ-XQLPTFJDSA-N tau-cadinol Chemical compound C1CC(C)=C[C@H]2[C@H](C(C)C)CC[C@](C)(O)[C@@H]21 LHYHMMRYTDARSZ-XQLPTFJDSA-N 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 2
150000003573 thiols Chemical class 0.000 description 2
WXQGPFZDVCRBME-UHFFFAOYSA-N thujopsene Natural products CC1=CCC2(C)CCCC(C)(C)C22C1C2 WXQGPFZDVCRBME-UHFFFAOYSA-N 0.000 description 2
125000003944 tolyl group Chemical group 0.000 description 2
CTMHWPIWNRWQEG-UHFFFAOYSA-N trans cyclohexenyl ester Natural products CC1=CCCCC1 CTMHWPIWNRWQEG-UHFFFAOYSA-N 0.000 description 2
KXSDPILWMGFJMM-UHFFFAOYSA-N trans-sabinene hydrate Natural products CC1(O)CCC2(C(C)C)C1C2 KXSDPILWMGFJMM-UHFFFAOYSA-N 0.000 description 2
YHBUQBJHSRGZNF-UHFFFAOYSA-N trans-α-Bisabolene Chemical compound CC(C)=CCC=C(C)C1CCC(C)=CC1 YHBUQBJHSRGZNF-UHFFFAOYSA-N 0.000 description 2
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 2
PZSJOBKRSVRODF-UHFFFAOYSA-N vanillin acetate Chemical compound COC1=CC(C=O)=CC=C1OC(C)=O PZSJOBKRSVRODF-UHFFFAOYSA-N 0.000 description 2
239000008158 vegetable oil Substances 0.000 description 2
235000013311 vegetables Nutrition 0.000 description 2
238000005406 washing Methods 0.000 description 2
HZRFVTRTTXBHSE-AYJHFOLZSA-N α-cedrene epoxide Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1C1(C)OC1C2 HZRFVTRTTXBHSE-AYJHFOLZSA-N 0.000 description 2
VMYXUZSZMNBRCN-UHFFFAOYSA-N α-curcumene Chemical compound CC(C)=CCCC(C)C1=CC=C(C)C=C1 VMYXUZSZMNBRCN-UHFFFAOYSA-N 0.000 description 2
SFEOKXHPFMOVRM-BQYQJAHWSA-N γ-ionone Chemical compound CC(=O)\C=C\C1C(=C)CCCC1(C)C SFEOKXHPFMOVRM-BQYQJAHWSA-N 0.000 description 2
FQTLCLSUCSAZDY-UHFFFAOYSA-N (+) E(S) nerolidol Natural products CC(C)=CCCC(C)=CCCC(C)(O)C=C FQTLCLSUCSAZDY-UHFFFAOYSA-N 0.000 description 1
WTVHAMTYZJGJLJ-UHFFFAOYSA-N (+)-(4S,8R)-8-epi-beta-bisabolol Natural products CC(C)=CCCC(C)C1(O)CCC(C)=CC1 WTVHAMTYZJGJLJ-UHFFFAOYSA-N 0.000 description 1
229930006718 (+)-alpha-pinene Natural products 0.000 description 1
OPFTUNCRGUEPRZ-UHFFFAOYSA-N (+)-beta-Elemen Natural products CC(=C)C1CCC(C)(C=C)C(C(C)=C)C1 OPFTUNCRGUEPRZ-UHFFFAOYSA-N 0.000 description 1
FUQAYSQLAOJBBC-UHFFFAOYSA-N (+)-caryolan-1-ol Natural products C1CC(C2)(C)CCCC2(O)C2CC(C)(C)C21 FUQAYSQLAOJBBC-UHFFFAOYSA-N 0.000 description 1
229930007022 (+)-dihydrocarveol Natural products 0.000 description 1
NDVASEGYNIMXJL-NXEZZACHSA-N (+)-sabinene Natural products C=C1CC[C@@]2(C(C)C)[C@@H]1C2 NDVASEGYNIMXJL-NXEZZACHSA-N 0.000 description 1
LFJQCDVYDGGFCH-JTQLQIEISA-N (+)-β-phellandrene Chemical compound CC(C)[C@@H]1CCC(=C)C=C1 LFJQCDVYDGGFCH-JTQLQIEISA-N 0.000 description 1
LFJQCDVYDGGFCH-SNVBAGLBSA-N (+/-)-beta-Phellandrene Natural products CC(C)[C@H]1CCC(=C)C=C1 LFJQCDVYDGGFCH-SNVBAGLBSA-N 0.000 description 1
GAIBLDCXCZKKJE-QRYCCKSOSA-N (-)-Germacrene D Natural products C(C)(C)[C@H]1/C=C/C(=C)CC/C=C(/C)\CC1 GAIBLDCXCZKKJE-QRYCCKSOSA-N 0.000 description 1
WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 1
229930007105 (-)-alpha-thujone Natural products 0.000 description 1
JLPUXFOGCDVKGO-TUAOUCFPSA-N (-)-geosmin Chemical compound C1CCC[C@]2(O)[C@@H](C)CCC[C@]21C JLPUXFOGCDVKGO-TUAOUCFPSA-N 0.000 description 1
CQUAYTJDLQBXCQ-NHYWBVRUSA-N (-)-isolongifolene Chemical compound C([C@@H](C1)C2(C)C)C[C@]31C2=CCCC3(C)C CQUAYTJDLQBXCQ-NHYWBVRUSA-N 0.000 description 1
GEWDNTWNSAZUDX-WQMVXFAESA-N (-)-methyl jasmonate Chemical compound CC\C=C/C[C@@H]1[C@@H](CC(=O)OC)CCC1=O GEWDNTWNSAZUDX-WQMVXFAESA-N 0.000 description 1
229930007631 (-)-perillyl alcohol Natural products 0.000 description 1
GXEGJTGWYVZSNR-UHFFFAOYSA-N (1E,4Z)-germacrene B Chemical compound CC(C)=C1CCC(C)=CCCC(C)=CC1 GXEGJTGWYVZSNR-UHFFFAOYSA-N 0.000 description 1
239000001871 (1R,2R,5S)-5-methyl-2-prop-1-en-2-ylcyclohexan-1-ol Substances 0.000 description 1
QMAYBMKBYCGXDH-KFWWJZLASA-N (1r,4as,8ar)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalene Chemical compound C1CC(C)=C[C@H]2[C@@H](C(C)C)CC=C(C)[C@H]21 QMAYBMKBYCGXDH-KFWWJZLASA-N 0.000 description 1
JXKJVDOCUVSQLC-UHFFFAOYSA-N (2-morpholin-4-ium-4-ylcyclohexyl) n-(2-chlorophenyl)carbamate;chloride Chemical compound [Cl-].ClC1=CC=CC=C1NC(=O)OC1C([NH+]2CCOCC2)CCCC1 JXKJVDOCUVSQLC-UHFFFAOYSA-N 0.000 description 1
239000001695 (2E)-1,1-dimethoxy-3,7-dimethylocta-2,6-diene Substances 0.000 description 1
NTWSIWWJPQHFTO-AATRIKPKSA-N (2E)-3-methylhex-2-enoic acid Chemical compound CCC\C(C)=C\C(O)=O NTWSIWWJPQHFTO-AATRIKPKSA-N 0.000 description 1
MBDOYVRWFFCFHM-SNAWJCMRSA-N (2E)-hexenal Chemical compound CCC\C=C\C=O MBDOYVRWFFCFHM-SNAWJCMRSA-N 0.000 description 1
HZYHMHHBBBSGHB-UHFFFAOYSA-N (2E,6E)-2,6-Nonadienal Natural products CCC=CCCC=CC=O HZYHMHHBBBSGHB-UHFFFAOYSA-N 0.000 description 1
NOPLRNXKHZRXHT-UHFFFAOYSA-N (2E,6E)-2,6-dimethyl-10-methylene-dodeca-2,6,11-trienal Natural products O=CC(C)=CCCC(C)=CCCC(=C)C=C NOPLRNXKHZRXHT-UHFFFAOYSA-N 0.000 description 1
239000001500 (2R)-6-methyl-2-[(1R)-4-methyl-1-cyclohex-3-enyl]hept-5-en-2-ol Substances 0.000 description 1
239000001890 (2R)-8,8,8a-trimethyl-2-prop-1-en-2-yl-1,2,3,4,6,7-hexahydronaphthalene Substances 0.000 description 1
NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 1
HPZWSJQQCJZBBG-UHFFFAOYSA-N (3E,5E)-2,6-dimethyl-1,3,5,7-octatetraene Natural products CC(=C)C=CC=C(C)C=C HPZWSJQQCJZBBG-UHFFFAOYSA-N 0.000 description 1
OSUJYLRDFDGEHZ-BLOPKESVSA-N (3Z)-3,7-dimethylocta-1,3,6-triene Chemical compound C/C(/C=C)=C/CC=C(C)C.C/C(/C=C)=C/CC=C(C)C OSUJYLRDFDGEHZ-BLOPKESVSA-N 0.000 description 1
JQQDKNVOSLONRS-JEGFTUTRSA-N (3e,5e)-undeca-1,3,5-triene Chemical compound CCCCC\C=C\C=C\C=C JQQDKNVOSLONRS-JEGFTUTRSA-N 0.000 description 1
NGSZDVVHIGAMOJ-YHYXMXQVSA-N (3z)-3-propylidene-2-benzofuran-1-one Chemical compound C1=CC=C2C(=C/CC)/OC(=O)C2=C1 NGSZDVVHIGAMOJ-YHYXMXQVSA-N 0.000 description 1
OUCCVXVYGFBXSV-UHFFFAOYSA-N (4-chlorophenyl)sulfanylmethylsulfanyl-dimethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound COP(=S)(OC)SCSC1=CC=C(Cl)C=C1 OUCCVXVYGFBXSV-UHFFFAOYSA-N 0.000 description 1
239000001075 (4R,4aR,8aS)-4,8a-dimethyl-1,2,3,4,5,6,7,8-octahydronaphthalen-4a-ol Substances 0.000 description 1
ZTJZJYUGOJYHCU-RMKNXTFCSA-N (5r,6s)-5,6-epoxy-7-megastigmen-9-one Chemical compound C1CCC(C)(C)C2(/C=C/C(=O)C)C1(C)O2 ZTJZJYUGOJYHCU-RMKNXTFCSA-N 0.000 description 1
OJUDXKATOGUCJX-ZRDIBKRKSA-N (6E)-3,7-dimethyldeca-1,6-diene Chemical compound C/C(/CCC)=C\CCC(C=C)C OJUDXKATOGUCJX-ZRDIBKRKSA-N 0.000 description 1
OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
WTTJVINHCBCLGX-UHFFFAOYSA-N (9trans,12cis)-methyl linoleate Natural products CCCCCC=CCC=CCCCCCCCC(=O)OC WTTJVINHCBCLGX-UHFFFAOYSA-N 0.000 description 1
125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
125000003161 (C1-C6) alkylene group Chemical group 0.000 description 1
YHBUQBJHSRGZNF-VGOFMYFVSA-N (E)-alpha-bisabolene Chemical compound CC(C)=CC\C=C(/C)C1CCC(C)=CC1 YHBUQBJHSRGZNF-VGOFMYFVSA-N 0.000 description 1
239000001714 (E)-hex-2-en-1-ol Substances 0.000 description 1
CXENHBSYCFFKJS-VDQVFBMKSA-N (E,E)-alpha-farnesene Chemical compound CC(C)=CCC\C(C)=C\C\C=C(/C)C=C CXENHBSYCFFKJS-VDQVFBMKSA-N 0.000 description 1
IDFPQEHZYBXIFO-GFCCVEGCSA-N (R)-(4-fluoro-2-propylphenyl)-(1H-imidazol-2-yl)methanol Chemical compound CCCc1cc(F)ccc1[C@@H](O)c1ncc[nH]1 IDFPQEHZYBXIFO-GFCCVEGCSA-N 0.000 description 1
DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
NEHNMFOYXAPHSD-JTQLQIEISA-N (S)-(-)-Citronellal Chemical compound O=CC[C@@H](C)CCC=C(C)C NEHNMFOYXAPHSD-JTQLQIEISA-N 0.000 description 1
229930004024 (S)-(-)-citronellol Natural products 0.000 description 1
235000018285 (S)-(-)-citronellol Nutrition 0.000 description 1
PAEBAEDUARAOSG-VOTSOKGWSA-N (Z)-1-(1-Ethoxyethoxy)-3-hexene Chemical compound CCOC(C)OCC\C=C\CC PAEBAEDUARAOSG-VOTSOKGWSA-N 0.000 description 1
RUJPNZNXGCHGID-UHFFFAOYSA-N (Z)-beta-Terpineol Natural products CC(=C)C1CCC(C)(O)CC1 RUJPNZNXGCHGID-UHFFFAOYSA-N 0.000 description 1
DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 1
CBVWMGCJNPPAAR-HJWRWDBZSA-N (nz)-n-(5-methylheptan-3-ylidene)hydroxylamine Chemical compound CCC(C)C\C(CC)=N/O CBVWMGCJNPPAAR-HJWRWDBZSA-N 0.000 description 1
WLALVCDHIGUUDM-UHFFFAOYSA-N 1,1,2,2,3,3-hexamethylindene Chemical compound C1=CC=C2C(C)(C)C(C)(C)C(C)(C)C2=C1 WLALVCDHIGUUDM-UHFFFAOYSA-N 0.000 description 1
ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
ARYLQJDBHZSMJJ-UHFFFAOYSA-N 1,2,3,3a,5,6-hexahydroinden-4-one Chemical compound O=C1CCC=C2CCCC12 ARYLQJDBHZSMJJ-UHFFFAOYSA-N 0.000 description 1
COWCJTPCHIGSPT-UHFFFAOYSA-N 1,2,3,4-tetrahydronaphthalene-2-carbonitrile Chemical compound C1=CC=C2CC(C#N)CCC2=C1 COWCJTPCHIGSPT-UHFFFAOYSA-N 0.000 description 1
ZGYZCSRPTRJWLK-UHFFFAOYSA-N 1,2,3,7,8,8a-hexahydronaphthalene Chemical compound C1=CCCC2CCCC=C21 ZGYZCSRPTRJWLK-UHFFFAOYSA-N 0.000 description 1
NAURBMSAOLUBCZ-UHFFFAOYSA-N 1,2-dioxaspiro[4.5]decane Chemical compound O1OCCC11CCCCC1 NAURBMSAOLUBCZ-UHFFFAOYSA-N 0.000 description 1
IFPMZBBHBZQTOV-UHFFFAOYSA-N 1,3,5-trinitro-2-(2,4,6-trinitrophenyl)-4-[2,4,6-trinitro-3-(2,4,6-trinitrophenyl)phenyl]benzene Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(C=2C(=C(C=3C(=CC(=CC=3[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O)C(=CC=2[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O)=C1[N+]([O-])=O IFPMZBBHBZQTOV-UHFFFAOYSA-N 0.000 description 1
WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
OPNDWUNGMWNXNB-UHFFFAOYSA-N 1,5-benzodioxepin-3-one Chemical compound O1CC(=O)COC2=CC=CC=C21 OPNDWUNGMWNXNB-UHFFFAOYSA-N 0.000 description 1
WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 1
VPKMGDRERYMTJX-CMDGGOBGSA-N 1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-1-penten-3-one Chemical compound CCC(=O)\C=C\C1C(C)=CCCC1(C)C VPKMGDRERYMTJX-CMDGGOBGSA-N 0.000 description 1
KVYVAGCVKWBOBS-UHFFFAOYSA-N 1-(4-chlorophenoxy)-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1OC1=CC=C(Cl)C=C1 KVYVAGCVKWBOBS-UHFFFAOYSA-N 0.000 description 1
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
XBGUIVFBMBVUEG-UHFFFAOYSA-N 1-methyl-4-(1,5-dimethyl-4-hexenylidene)-1-cyclohexene Chemical compound CC(C)=CCCC(C)=C1CCC(C)=CC1 XBGUIVFBMBVUEG-UHFFFAOYSA-N 0.000 description 1
KFGBSCFOJPHENY-UHFFFAOYSA-N 1-oxacycloheptadec-9-en-2-one Chemical compound O=C1CCCCCCC=CCCCCCCCO1 KFGBSCFOJPHENY-UHFFFAOYSA-N 0.000 description 1
239000001875 1-phenylethyl acetate Substances 0.000 description 1
ZNJHENRZPYCHJO-UHFFFAOYSA-N 1-propan-2-ylbenzotriazole-5-carbonyl chloride Chemical compound ClC(=O)C1=CC=C2N(C(C)C)N=NC2=C1 ZNJHENRZPYCHJO-UHFFFAOYSA-N 0.000 description 1
MQENMJWOIDRKBG-UHFFFAOYSA-N 11-oxabicyclo[10.1.0]trideca-4,8-diene Chemical compound C1CC=CCCC=CCOC2CC21 MQENMJWOIDRKBG-UHFFFAOYSA-N 0.000 description 1
229940114072 12-hydroxystearic acid Drugs 0.000 description 1
FOSDFRQPYFEJEH-UHFFFAOYSA-N 1h-inden-1-yl acetate Chemical compound C1=CC=C2C(OC(=O)C)C=CC2=C1 FOSDFRQPYFEJEH-UHFFFAOYSA-N 0.000 description 1
YSXYEWMLRICGIF-UHFFFAOYSA-N 2,3,4,5-tetrahydro-1h-1,4-benzodiazepin-8-ylmethanol Chemical compound C1NCCNC2=CC(CO)=CC=C21 YSXYEWMLRICGIF-UHFFFAOYSA-N 0.000 description 1
YGBXXWTZWLALGR-UHFFFAOYSA-N 2,3-Dimethylbenzofuran Chemical compound C1=CC=C2C(C)=C(C)OC2=C1 YGBXXWTZWLALGR-UHFFFAOYSA-N 0.000 description 1
RIZUCYSQUWMQLX-UHFFFAOYSA-N 2,3-dimethylbenzoic acid Chemical compound CC1=CC=CC(C(O)=O)=C1C RIZUCYSQUWMQLX-UHFFFAOYSA-N 0.000 description 1
AMOYMEBHYUTMKJ-UHFFFAOYSA-N 2-(2-phenylethoxy)ethylbenzene Chemical compound C=1C=CC=CC=1CCOCCC1=CC=CC=C1 AMOYMEBHYUTMKJ-UHFFFAOYSA-N 0.000 description 1
FACFHHMQICTXFZ-UHFFFAOYSA-N 2-(2-phenylimidazo[1,2-a]pyridin-3-yl)ethanamine Chemical compound N1=C2C=CC=CN2C(CCN)=C1C1=CC=CC=C1 FACFHHMQICTXFZ-UHFFFAOYSA-N 0.000 description 1
VVUMWAHNKOLVSN-UHFFFAOYSA-N 2-(4-ethoxyanilino)-n-propylpropanamide Chemical compound CCCNC(=O)C(C)NC1=CC=C(OCC)C=C1 VVUMWAHNKOLVSN-UHFFFAOYSA-N 0.000 description 1
239000001952 2-(4-methyl-1-cyclohex-3-enyl)propan-2-yl propanoate Substances 0.000 description 1
239000001278 2-(5-ethenyl-5-methyloxolan-2-yl)propan-2-ol Substances 0.000 description 1
SSICPQZWCDZSQA-UHFFFAOYSA-N 2-(methoxymethyl)phenol Chemical compound COCC1=CC=CC=C1O SSICPQZWCDZSQA-UHFFFAOYSA-N 0.000 description 1
LKAWQFHWVVSFTR-UHFFFAOYSA-N 2-(methylamino)ethanol;hydrochloride Chemical compound [Cl-].C[NH2+]CCO LKAWQFHWVVSFTR-UHFFFAOYSA-N 0.000 description 1
GNRKVLMFBDYHJW-UHFFFAOYSA-N 2-(methylamino)ethanol;methyl hydrogen sulfate Chemical compound C[NH2+]CCO.COS([O-])(=O)=O GNRKVLMFBDYHJW-UHFFFAOYSA-N 0.000 description 1
RADIRXJQODWKGQ-HWKANZROSA-N 2-Ethoxy-5-(1-propenyl)phenol Chemical compound CCOC1=CC=C(\C=C\C)C=C1O RADIRXJQODWKGQ-HWKANZROSA-N 0.000 description 1
GVONPEQEUQYVNH-SNAWJCMRSA-N 2-Methyl-3-(2-pentenyl)-2-cyclopenten-1-one Chemical compound CC\C=C\CC1=C(C)C(=O)CC1 GVONPEQEUQYVNH-SNAWJCMRSA-N 0.000 description 1
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
NDLNTMNRNCENRZ-UHFFFAOYSA-N 2-[2-hydroxyethyl(octadecyl)amino]ethanol Chemical compound CCCCCCCCCCCCCCCCCCN(CCO)CCO NDLNTMNRNCENRZ-UHFFFAOYSA-N 0.000 description 1
SSZACLYPEFCREM-UHFFFAOYSA-N 2-benzyl-1,3-dioxolane Chemical compound C=1C=CC=CC=1CC1OCCO1 SSZACLYPEFCREM-UHFFFAOYSA-N 0.000 description 1
239000001065 2-benzylideneheptyl acetate Substances 0.000 description 1
GOLVMRZULJWHGT-UHFFFAOYSA-N 2-cyclohexyloxyacetic acid Chemical compound OC(=O)COC1CCCCC1 GOLVMRZULJWHGT-UHFFFAOYSA-N 0.000 description 1
PJISLFCKHOHLLP-UHFFFAOYSA-N 2-diethoxyphosphorylsulfanyl-n,n-diethylethanamine Chemical compound CCOP(=O)(OCC)SCCN(CC)CC PJISLFCKHOHLLP-UHFFFAOYSA-N 0.000 description 1
ZCHHRLHTBGRGOT-UHFFFAOYSA-N 2-hexen-1-ol Chemical compound CCCC=CCO ZCHHRLHTBGRGOT-UHFFFAOYSA-N 0.000 description 1
WZPGQHVPSKTELT-YFHOEESVSA-N 2-hexylidenecyclopentanone Chemical compound CCCCC\C=C1\CCCC1=O WZPGQHVPSKTELT-YFHOEESVSA-N 0.000 description 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
VFAARUJMGUIZDA-AWLASTDMSA-N 2-hydroxyethyl-bis[2-[(z)-octadec-9-enoxy]ethyl]azanium;methyl sulfate Chemical compound COS([O-])(=O)=O.CCCCCCCC\C=C/CCCCCCCCOCC[NH+](CCO)CCOCCCCCCCC\C=C/CCCCCCCC VFAARUJMGUIZDA-AWLASTDMSA-N 0.000 description 1
CRNOHKQARKZYBD-UHFFFAOYSA-N 2-hydroxyethyl-methyl-bis[2-[[(Z)-octadec-9-enoyl]amino]ethyl]azanium methyl sulfate Chemical compound S(=O)(=O)(OC)[O-].C[N+](CCO)(CCNC(CCCCCCCC=C/CCCCCCCC)=O)CCNC(CCCCCCCC=C/CCCCCCCC)=O CRNOHKQARKZYBD-UHFFFAOYSA-N 0.000 description 1
SPRJWMSXOLZOIO-UHFFFAOYSA-N 2-hydroxypropanoyl octanoate Chemical compound CCCCCCCC(=O)OC(=O)C(C)O SPRJWMSXOLZOIO-UHFFFAOYSA-N 0.000 description 1
IOLQAHFPDADCHJ-UXBLZVDNSA-N 2-isopropyl-5-methyl-2-hexenal Chemical compound CC(C)C\C=C(/C=O)C(C)C IOLQAHFPDADCHJ-UXBLZVDNSA-N 0.000 description 1
SGVBCLGVIOFAFT-UHFFFAOYSA-N 2-methyl-3-(4-methylphenyl)propanal Chemical compound O=CC(C)CC1=CC=C(C)C=C1 SGVBCLGVIOFAFT-UHFFFAOYSA-N 0.000 description 1
HLMACKQLXSEXIY-UHFFFAOYSA-N 2-methyldec-1-ene Chemical compound CCCCCCCCC(C)=C HLMACKQLXSEXIY-UHFFFAOYSA-N 0.000 description 1
ZBSDPCQVZJAOGX-UHFFFAOYSA-N 2-methylidenecyclohexane-1-carboxylic acid Chemical compound OC(=O)C1CCCCC1=C ZBSDPCQVZJAOGX-UHFFFAOYSA-N 0.000 description 1
YBDQLHBVNXARAU-UHFFFAOYSA-N 2-methyloxane Chemical compound CC1CCCCO1 YBDQLHBVNXARAU-UHFFFAOYSA-N 0.000 description 1
JYVLIDXNZAXMDK-UHFFFAOYSA-N 2-pentanol Substances CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 description 1
QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 1
UNFGQCCHVMMMRF-UHFFFAOYSA-N 2-phenylbutanamide Chemical compound CCC(C(N)=O)C1=CC=CC=C1 UNFGQCCHVMMMRF-UHFFFAOYSA-N 0.000 description 1
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
TZYYJCQVZHDEMI-UHFFFAOYSA-N 2-phenyloxolane Chemical compound C1CCOC1C1=CC=CC=C1 TZYYJCQVZHDEMI-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
ZPSJGADGUYYRKE-UHFFFAOYSA-N 2H-pyran-2-one Chemical compound O=C1C=CC=CO1 ZPSJGADGUYYRKE-UHFFFAOYSA-N 0.000 description 1
239000001629 3,7-dimethylocta-2,6-dienyl benzoate Substances 0.000 description 1
LNJCGNRKWOHFFV-UHFFFAOYSA-N 3-(2-hydroxyethylsulfanyl)propanenitrile Chemical compound OCCSCCC#N LNJCGNRKWOHFFV-UHFFFAOYSA-N 0.000 description 1
BWVZAZPLUTUBKD-UHFFFAOYSA-N 3-(5,6,6-Trimethylbicyclo[2.2.1]hept-1-yl)cyclohexanol Chemical compound CC1(C)C(C)C2CC1CC2C1CCCC(O)C1 BWVZAZPLUTUBKD-UHFFFAOYSA-N 0.000 description 1
GTNCESCYZPMXCJ-UHFFFAOYSA-N 3-Phenylpropyl propanoate Chemical compound CCC(=O)OCCCC1=CC=CC=C1 GTNCESCYZPMXCJ-UHFFFAOYSA-N 0.000 description 1
GVSTVIASYRSHQM-RYUDHWBXSA-N 3-[(1s,5r)-6,6-dimethyl-4-bicyclo[3.1.1]hept-3-enyl]-2,2-dimethylpropanal Chemical compound C1[C@@]2([H])C(CC(C)(C)C=O)=CC[C@]1([H])C2(C)C GVSTVIASYRSHQM-RYUDHWBXSA-N 0.000 description 1
AGNTUZCMJBTHOG-UHFFFAOYSA-N 3-[3-(2,3-dihydroxypropoxy)-2-hydroxypropoxy]propane-1,2-diol Chemical compound OCC(O)COCC(O)COCC(O)CO AGNTUZCMJBTHOG-UHFFFAOYSA-N 0.000 description 1
MUNHWMPRAFMHQA-UHFFFAOYSA-N 3-[dodecyl(3-hydroxypropyl)amino]propan-1-ol Chemical compound CCCCCCCCCCCCN(CCCO)CCCO MUNHWMPRAFMHQA-UHFFFAOYSA-N 0.000 description 1
RHPXYZMDLOJTFF-UHFFFAOYSA-N 3-amino-4-hydroxy-5-nitrobenzenesulfonic acid Chemical compound NC1=CC(S(O)(=O)=O)=CC([N+]([O-])=O)=C1O RHPXYZMDLOJTFF-UHFFFAOYSA-N 0.000 description 1
CLYAQFSQLQTVNO-UHFFFAOYSA-N 3-cyclohexylpropan-1-ol Chemical compound OCCCC1CCCCC1 CLYAQFSQLQTVNO-UHFFFAOYSA-N 0.000 description 1
AIQLNKITFBJPFO-UHFFFAOYSA-N 3-hexenyl isovalerate Chemical compound CCC=CCCOC(=O)CC(C)C AIQLNKITFBJPFO-UHFFFAOYSA-N 0.000 description 1
RLAOJKCSTGZACZ-UHFFFAOYSA-N 3-methylcyclopentadec-2-en-1-one Chemical compound CC1=CC(=O)CCCCCCCCCCCC1 RLAOJKCSTGZACZ-UHFFFAOYSA-N 0.000 description 1
NGSZDVVHIGAMOJ-UHFFFAOYSA-N 3-propylidene-2-benzofuran-1-one Chemical compound C1=CC=C2C(=CCC)OC(=O)C2=C1 NGSZDVVHIGAMOJ-UHFFFAOYSA-N 0.000 description 1
GNIXIZIBODKFLK-UHFFFAOYSA-N 4,4-dimethylpentanamide Chemical compound CC(C)(C)CCC(N)=O GNIXIZIBODKFLK-UHFFFAOYSA-N 0.000 description 1
RUNKSQBQFFBFPZ-UHFFFAOYSA-N 4,7-methanoindene Chemical compound C1C2=C3CC=CC3=C1C=C2 RUNKSQBQFFBFPZ-UHFFFAOYSA-N 0.000 description 1
OOAPBGPLZAFZSO-UHFFFAOYSA-N 4-(2-chloroethyl)benzoic acid Chemical compound OC(=O)C1=CC=C(CCCl)C=C1 OOAPBGPLZAFZSO-UHFFFAOYSA-N 0.000 description 1
TZJLGGWGVLADDN-UHFFFAOYSA-N 4-(3,4-Methylenedioxyphenyl)-2-butanone Chemical compound CC(=O)CCC1=CC=C2OCOC2=C1 TZJLGGWGVLADDN-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
ZQVKTHRQIXSMGY-UHFFFAOYSA-N 4-Ethylbenzoic acid Chemical compound CCC1=CC=C(C(O)=O)C=C1 ZQVKTHRQIXSMGY-UHFFFAOYSA-N 0.000 description 1
CDPKJZJVTHSESZ-UHFFFAOYSA-N 4-chlorophenylacetic acid Chemical compound OC(=O)CC1=CC=C(Cl)C=C1 CDPKJZJVTHSESZ-UHFFFAOYSA-N 0.000 description 1
MBVFRSJFKMJRHA-UHFFFAOYSA-N 4-fluoro-1-benzofuran-7-carbaldehyde Chemical compound FC1=CC=C(C=O)C2=C1C=CO2 MBVFRSJFKMJRHA-UHFFFAOYSA-N 0.000 description 1
HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
WYSYRGOYGZBCLG-UHFFFAOYSA-N 4-methylidenebicyclo[3.3.1]nonane Chemical compound C1CCC2C(=C)CCC1C2 WYSYRGOYGZBCLG-UHFFFAOYSA-N 0.000 description 1
OTLNPYWUJOZPPA-UHFFFAOYSA-N 4-nitrobenzoic acid Chemical compound OC(=O)C1=CC=C([N+]([O-])=O)C=C1 OTLNPYWUJOZPPA-UHFFFAOYSA-N 0.000 description 1
NQMGELVSLIQQOI-UHFFFAOYSA-N 4-oxabicyclo[3.2.1]octane Chemical compound C1C2CCC1OCC2 NQMGELVSLIQQOI-UHFFFAOYSA-N 0.000 description 1
RMCHMXPTUMFFBZ-UHFFFAOYSA-N 5-bromo-1-methylindazole Chemical compound BrC1=CC=C2N(C)N=CC2=C1 RMCHMXPTUMFFBZ-UHFFFAOYSA-N 0.000 description 1
XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
VJSRZKPJIRNEIC-UHFFFAOYSA-N 6-methoxy-1,2,3,4,5,7-hexahydrotricyclo[2.2.1.0^{2,6}]heptane Chemical compound C1C2C3(OC)C2CC1C3 VJSRZKPJIRNEIC-UHFFFAOYSA-N 0.000 description 1
ODRDTKMYQDXVGG-UHFFFAOYSA-N 8-methoxycoumarin Natural products C1=CC(=O)OC2=C1C=CC=C2OC ODRDTKMYQDXVGG-UHFFFAOYSA-N 0.000 description 1
LLVFKEOMLYDSGT-FARCUNLSSA-N 9-ethylidene-3-oxatricyclo(6.2.1.02,7)undecane-4-one Chemical compound C12CCC(=O)OC2C2C\C(=C/C)C1C2 LLVFKEOMLYDSGT-FARCUNLSSA-N 0.000 description 1
101100383234 Acremonium chrysogenum CEFG gene Proteins 0.000 description 1
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 1
241000251468 Actinopterygii Species 0.000 description 1
241000234282 Allium Species 0.000 description 1
235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
244000016163 Allium sibiricum Species 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
WUNJOFRDOLDAOY-AATRIKPKSA-N Anapear Chemical compound COC(=O)CC\C=C\CC=C WUNJOFRDOLDAOY-AATRIKPKSA-N 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
RRNIZKPFKNDSRS-UHFFFAOYSA-N Bensulide Chemical compound CC(C)OP(=S)(OC(C)C)SCCNS(=O)(=O)C1=CC=CC=C1 RRNIZKPFKNDSRS-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
235000014698 Brassica juncea var multisecta Nutrition 0.000 description 1
235000006008 Brassica napus var napus Nutrition 0.000 description 1
235000006618 Brassica rapa subsp oleifera Nutrition 0.000 description 1
244000188595 Brassica sinapistrum Species 0.000 description 1
206010006326 Breath odour Diseases 0.000 description 1
LGOFSGDSFQNIAT-UHFFFAOYSA-N Bulnesol Natural products C1CC(C(C)(C)O)CC2C(C)CCC2=C1C LGOFSGDSFQNIAT-UHFFFAOYSA-N 0.000 description 1
239000004322 Butylated hydroxytoluene Substances 0.000 description 1
XHVLCJCTGJALLO-UHFFFAOYSA-N C(CCCC)OC(=O)C1C=CCCC1 Chemical compound C(CCCC)OC(=O)C1C=CCCC1 XHVLCJCTGJALLO-UHFFFAOYSA-N 0.000 description 1
LOMJIARXOSKCPS-UHFFFAOYSA-N CC(O)CO.CCCCCCCC(C)=O Chemical compound CC(O)CO.CCCCCCCC(C)=O LOMJIARXOSKCPS-UHFFFAOYSA-N 0.000 description 1
JIRBTIZDRVEGAZ-UHFFFAOYSA-N CC1CC(O)C2CCCC2C2C(C)(C)C12C Chemical compound CC1CC(O)C2CCCC2C2C(C)(C)C12C JIRBTIZDRVEGAZ-UHFFFAOYSA-N 0.000 description 1
VWFXPROOUAWFEE-NTBGYTOLSA-N CC1C[C@H]2C3CCC(C3)[C@H]2CC1=O Chemical compound CC1C[C@H]2C3CCC(C3)[C@H]2CC1=O VWFXPROOUAWFEE-NTBGYTOLSA-N 0.000 description 1
FWRHUQUOXUBCJB-UHFFFAOYSA-N CC=1C=C2OC(=C(C22C(=C(C(=C2C=1C)C)C)C)C)C Chemical compound CC=1C=C2OC(=C(C22C(=C(C(=C2C=1C)C)C)C)C)C FWRHUQUOXUBCJB-UHFFFAOYSA-N 0.000 description 1
YVADRFUQEMLGRC-UHFFFAOYSA-L CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC.CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC.COS(=O)(=O)[O-].COS(=O)(=O)[O-] Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC.CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC.COS(=O)(=O)[O-].COS(=O)(=O)[O-] YVADRFUQEMLGRC-UHFFFAOYSA-L 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
101100197558 Candida maltosa RIM-C gene Proteins 0.000 description 1
101100197561 Candida tropicalis RPL44 gene Proteins 0.000 description 1
239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
239000005973 Carvone Substances 0.000 description 1
YTHRBOFHFYZBRJ-RYUDHWBXSA-N Carvyl acetate Natural products CC(=O)O[C@H]1C[C@@H](C(C)=C)CC=C1C YTHRBOFHFYZBRJ-RYUDHWBXSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
241000723346 Cinnamomum camphora Species 0.000 description 1
102100025567 Citron Rho-interacting kinase Human genes 0.000 description 1
101710087170 Citron rho-interacting kinase Proteins 0.000 description 1
241000207199 Citrus Species 0.000 description 1
244000183685 Citrus aurantium Species 0.000 description 1
235000007716 Citrus aurantium Nutrition 0.000 description 1
241000195493 Cryptophyta Species 0.000 description 1
VMYXUZSZMNBRCN-AWEZNQCLSA-N Curcumene Natural products CC(C)=CCC[C@H](C)C1=CC=C(C)C=C1 VMYXUZSZMNBRCN-AWEZNQCLSA-N 0.000 description 1
MAMMVUWCKMOLSG-UHFFFAOYSA-N Cyclohexyl propionate Chemical compound CCC(=O)OC1CCCCC1 MAMMVUWCKMOLSG-UHFFFAOYSA-N 0.000 description 1
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
XURCUMFVQKJMJP-UHFFFAOYSA-N Dihydro-alpha-guaien Natural products C1C(C(C)C)CCC(C)C2=C1C(C)CC2 XURCUMFVQKJMJP-UHFFFAOYSA-N 0.000 description 1
LLKXNMNOHBQSJW-UHFFFAOYSA-N Elemol Natural products CCC(=C)C1CC(C=CC1(C)C)C(C)(C)O LLKXNMNOHBQSJW-UHFFFAOYSA-N 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
241000402754 Erythranthe moschata Species 0.000 description 1
239000004386 Erythritol Substances 0.000 description 1
UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
239000001116 FEMA 4028 Substances 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
229920002907 Guar gum Polymers 0.000 description 1
244000020551 Helianthus annuus Species 0.000 description 1
235000003222 Helianthus annuus Nutrition 0.000 description 1
XMRKUJJDDKYUHV-UHFFFAOYSA-N Helminthogermacrene Natural products CC(=C)C1CCC(C)=CCCC(C)=CC1 XMRKUJJDDKYUHV-UHFFFAOYSA-N 0.000 description 1
JTCIUOKKVACNCK-YHYXMXQVSA-N Hexyl tiglate Natural products CCCCCCOC(=O)C(\C)=C/C JTCIUOKKVACNCK-YHYXMXQVSA-N 0.000 description 1
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
AEXLFXYEFLKADK-UHFFFAOYSA-N Isocyclocitral Chemical compound CC1CC(C)=CC(C)C1C=O.CC1C=C(C)CC(C=O)C1C AEXLFXYEFLKADK-UHFFFAOYSA-N 0.000 description 1
KLDXJTOLSGUMSJ-JGWLITMVSA-N Isosorbide Chemical group O[C@@H]1CO[C@@H]2[C@@H](O)CO[C@@H]21 KLDXJTOLSGUMSJ-JGWLITMVSA-N 0.000 description 1
ZBJCYZPANVLBRK-IGJPJIBNSA-N L-Menthone 1,2-glycerol ketal Chemical compound CC(C)[C@@H]1CC[C@@H](C)CC11OC(CO)CO1 ZBJCYZPANVLBRK-IGJPJIBNSA-N 0.000 description 1
241000207923 Lamiaceae Species 0.000 description 1
YDQJXVYGARVLRT-UHFFFAOYSA-N Lepidine Natural products C=1C=CC(CC=2NC=CN=2)=CC=1OC=1C(OC)=CC=CC=1CC1=NC=CN1 YDQJXVYGARVLRT-UHFFFAOYSA-N 0.000 description 1
UWKAYLJWKGQEPM-LBPRGKRZSA-N Linaloyl acetate Natural products CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 1
JBVVONYMRFACPQ-UHFFFAOYSA-N Linalylformate Natural products CC(=C)CCCC(C)(OC=O)C=C JBVVONYMRFACPQ-UHFFFAOYSA-N 0.000 description 1
OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
ACOBBFVLNKYODD-CSKARUKUSA-N Methyl geranate Chemical compound COC(=O)\C=C(/C)CCC=C(C)C ACOBBFVLNKYODD-CSKARUKUSA-N 0.000 description 1
PKIXXJPMNDDDOS-UHFFFAOYSA-N Methyl linoleate Natural products CCCCC=CCCC=CCCCCCCCC(=O)OC PKIXXJPMNDDDOS-UHFFFAOYSA-N 0.000 description 1
239000006001 Methyl nonyl ketone Substances 0.000 description 1
101000918894 Mus musculus Beta-defensin 8 Proteins 0.000 description 1
235000021360 Myristic acid Nutrition 0.000 description 1
RWAXQWRDVUOOGG-UHFFFAOYSA-N N,2,3-Trimethyl-2-(1-methylethyl)butanamide Chemical compound CNC(=O)C(C)(C(C)C)C(C)C RWAXQWRDVUOOGG-UHFFFAOYSA-N 0.000 description 1
FQTLCLSUCSAZDY-ATGUSINASA-N Nerolidol Chemical compound CC(C)=CCC\C(C)=C\CC[C@](C)(O)C=C FQTLCLSUCSAZDY-ATGUSINASA-N 0.000 description 1
JABWTTMMTQMDPW-UHFFFAOYSA-N O1COC2C1=C1C=CC=C1C=C2 Chemical compound O1COC2C1=C1C=CC=C1C=C2 JABWTTMMTQMDPW-UHFFFAOYSA-N 0.000 description 1
JRUVMYZHRMOZLW-UHFFFAOYSA-N O1OC(CCC2=C1C=CC=C2)=O Chemical compound O1OC(CCC2=C1C=CC=C2)=O JRUVMYZHRMOZLW-UHFFFAOYSA-N 0.000 description 1
SPNFHMLVXCPEFS-UHFFFAOYSA-N OC1=CC=C2CC2=C2C=CC=C12 Chemical compound OC1=CC=C2CC2=C2C=CC=C12 SPNFHMLVXCPEFS-UHFFFAOYSA-N 0.000 description 1
MSFLYJIWLHSQLG-UHFFFAOYSA-N Octahydro-2H-1-benzopyran-2-one Chemical compound C1CCCC2OC(=O)CCC21 MSFLYJIWLHSQLG-UHFFFAOYSA-N 0.000 description 1
235000019483 Peanut oil Nutrition 0.000 description 1
PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
240000004760 Pimpinella anisum Species 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
PXRCIOIWVGAZEP-UHFFFAOYSA-N Primaeres Camphenhydrat Natural products C1CC2C(O)(C)C(C)(C)C1C2 PXRCIOIWVGAZEP-UHFFFAOYSA-N 0.000 description 1
235000019484 Rapeseed oil Nutrition 0.000 description 1
235000019774 Rice Bran oil Nutrition 0.000 description 1
GJJYQFPADNKBDY-UHFFFAOYSA-N Sabinol Natural products C=C1CCC2(C(C)C)C1(O)C2 GJJYQFPADNKBDY-UHFFFAOYSA-N 0.000 description 1
240000004808 Saccharomyces cerevisiae Species 0.000 description 1
235000019485 Safflower oil Nutrition 0.000 description 1
BTANRVKWQNVYAZ-UHFFFAOYSA-N Sec-butyl alcohol Natural products CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 1
235000003434 Sesamum indicum Nutrition 0.000 description 1
244000040738 Sesamum orientale Species 0.000 description 1
229910020485 SiO4/2 Inorganic materials 0.000 description 1
244000028419 Styrax benzoin Species 0.000 description 1
235000000126 Styrax benzoin Nutrition 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
235000008411 Sumatra benzointree Nutrition 0.000 description 1
235000019486 Sunflower oil Nutrition 0.000 description 1
DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 1
239000005844 Thymol Substances 0.000 description 1
BAECOWNUKCLBPZ-HIUWNOOHSA-N Triolein Natural products O([C@H](OCC(=O)CCCCCCC/C=C\CCCCCCCC)COC(=O)CCCCCCC/C=C\CCCCCCCC)C(=O)CCCCCCC/C=C\CCCCCCCC BAECOWNUKCLBPZ-HIUWNOOHSA-N 0.000 description 1
PHYFQTYBJUILEZ-UHFFFAOYSA-N Trioleoylglycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCCCCCCCC)COC(=O)CCCCCCCC=CCCCCCCCC PHYFQTYBJUILEZ-UHFFFAOYSA-N 0.000 description 1
TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
XJHRZBIBSSVCEL-UHFFFAOYSA-N Z-Non-6-en-1-ol Natural products CCC=CCCCCCO XJHRZBIBSSVCEL-UHFFFAOYSA-N 0.000 description 1
FAFMZORPAAGQFV-BREBYQMCSA-N [(1r,3r,4r)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] propanoate Chemical compound C1C[C@@]2(C)[C@H](OC(=O)CC)C[C@@H]1C2(C)C FAFMZORPAAGQFV-BREBYQMCSA-N 0.000 description 1
KGEKLUUHTZCSIP-UMNHJUIQSA-N [(1s,3r,4r)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] acetate Chemical compound C1C[C@@]2(C)[C@H](OC(=O)C)C[C@H]1C2(C)C KGEKLUUHTZCSIP-UMNHJUIQSA-N 0.000 description 1
IJCWFDPJFXGQBN-RYNSOKOISA-N [(2R)-2-[(2R,3R,4S)-4-hydroxy-3-octadecanoyloxyoxolan-2-yl]-2-octadecanoyloxyethyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCCCCCCCCCCCC IJCWFDPJFXGQBN-RYNSOKOISA-N 0.000 description 1
TTZKGYULRVDFJJ-GIVMLJSASA-N [(2r)-2-[(2s,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-[(z)-octadec-9-enoyl]oxyethyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1O TTZKGYULRVDFJJ-GIVMLJSASA-N 0.000 description 1
PZQBWGFCGIRLBB-NJYHNNHUSA-N [(2r)-2-[(2s,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-octadecanoyloxyethyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCCCC)[C@H]1OC[C@H](O)[C@H]1O PZQBWGFCGIRLBB-NJYHNNHUSA-N 0.000 description 1
DNTMJTROKXRBDM-UUWWDYFTSA-N [(2r,3r,4s)-2-[(1r)-1-hexadecanoyloxy-2-hydroxyethyl]-4-hydroxyoxolan-3-yl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)O[C@H](CO)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCCCCCCCCCC DNTMJTROKXRBDM-UUWWDYFTSA-N 0.000 description 1
MPKOLWUWOADQCX-BMRADRMJSA-N [(e)-2-(diethoxymethyl)hept-1-enyl]benzene Chemical compound CCCCC\C(C(OCC)OCC)=C/C1=CC=CC=C1 MPKOLWUWOADQCX-BMRADRMJSA-N 0.000 description 1
JNWQKXUWZWKUAY-BHHIIOOYSA-N [(z)-hex-3-enyl] (z)-2-methylbut-2-enoate Chemical compound CC\C=C/CCOC(=O)C(\C)=C/C JNWQKXUWZWKUAY-BHHIIOOYSA-N 0.000 description 1
238000005299 abrasion Methods 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
238000007259 addition reaction Methods 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000005250 alkyl acrylate group Chemical group 0.000 description 1
OOCCDEMITAIZTP-UHFFFAOYSA-N allylic benzylic alcohol Natural products OCC=CC1=CC=CC=C1 OOCCDEMITAIZTP-UHFFFAOYSA-N 0.000 description 1
CMJSVJIGLBDCME-VBKFSLOCSA-N alpha-Amylcinnamyl acetate Chemical compound CCCCC\C(COC(C)=O)=C\C1=CC=CC=C1 CMJSVJIGLBDCME-VBKFSLOCSA-N 0.000 description 1
RGZSQWQPBWRIAQ-LSDHHAIUSA-N alpha-Bisabolol Natural products CC(C)=CCC[C@@](C)(O)[C@@H]1CCC(C)=CC1 RGZSQWQPBWRIAQ-LSDHHAIUSA-N 0.000 description 1
KVQOADNSNSUAJT-NHULGOKLSA-N alpha-Patchoulene Natural products C[C@@H]1[C@H]2[C@]3(C(C)(C)[C@H](C2)CC=C3C)CC1 KVQOADNSNSUAJT-NHULGOKLSA-N 0.000 description 1
229930016183 alpha-curcumene Natural products 0.000 description 1
PSVBPLKYDMHILE-UHFFFAOYSA-N alpha-humulene Natural products CC1=C/CC(C)(C)C=CCC=CCC1 PSVBPLKYDMHILE-UHFFFAOYSA-N 0.000 description 1
PFSTYGCNVAVZBK-YHTQAGCZSA-N alpha-sinensal Natural products O=C/C(=C\CC/C(=C\C/C=C(\C=C)/C)/C)/C PFSTYGCNVAVZBK-YHTQAGCZSA-N 0.000 description 1
KQAZVFVOEIRWHN-UHFFFAOYSA-N alpha-thujene Natural products CC1=CCC2(C(C)C)C1C2 KQAZVFVOEIRWHN-UHFFFAOYSA-N 0.000 description 1
USMNOWBWPHYOEA-UHFFFAOYSA-N alpha-thujone Natural products CC1C(=O)CC2(C(C)C)C1C2 USMNOWBWPHYOEA-UHFFFAOYSA-N 0.000 description 1
229920013822 aminosilicone Polymers 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
239000002280 amphoteric surfactant Substances 0.000 description 1
239000003242 anti bacterial agent Substances 0.000 description 1
230000003466 anti-cipated effect Effects 0.000 description 1
239000012753 anti-shrinkage agent Substances 0.000 description 1
230000001153 anti-wrinkle effect Effects 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
DNAVOCNYHNNEQI-UHFFFAOYSA-N asaronaldehyde Natural products COC1=CC(OC)=C(C=CC=O)C=C1OC DNAVOCNYHNNEQI-UHFFFAOYSA-N 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
IPTLKMXBROVJJF-UHFFFAOYSA-N azanium;methyl sulfate Chemical compound N.COS(O)(=O)=O IPTLKMXBROVJJF-UHFFFAOYSA-N 0.000 description 1
235000015278 beef Nutrition 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
229960002130 benzoin Drugs 0.000 description 1
229960004217 benzyl alcohol Drugs 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
AVOZUZVXXIYSGL-UHFFFAOYSA-M benzyl-dimethyl-octadecylazanium;methyl sulfate Chemical compound COS([O-])(=O)=O.CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 AVOZUZVXXIYSGL-UHFFFAOYSA-M 0.000 description 1
229960002045 bergapten Drugs 0.000 description 1
NPCUVKWCXITFFV-UHFFFAOYSA-N beta-Himachalene Natural products CC1(C)CCCC2(CO2)C3CCC4(C)OC4C13 NPCUVKWCXITFFV-UHFFFAOYSA-N 0.000 description 1
OJYKYCDSGQGTRJ-INLOORNJSA-N beta-Santalol Natural products C1C[C@H]2C(=C)[C@](CC\C=C(CO)/C)(C)[C@@H]1C2 OJYKYCDSGQGTRJ-INLOORNJSA-N 0.000 description 1
PHWISBHSBNDZDX-UHFFFAOYSA-N beta-Sesquiphellandrene Natural products CC(C)=CCCC(C)C1CCC(=C)C=C1 PHWISBHSBNDZDX-UHFFFAOYSA-N 0.000 description 1
ISLOGSAEQNKPGG-UHFFFAOYSA-N beta-Vetivone Chemical compound CC1CC(=O)C=C(C)C11CC(=C(C)C)CC1 ISLOGSAEQNKPGG-UHFFFAOYSA-N 0.000 description 1
229940074775 beta-bisabolol Drugs 0.000 description 1
NPNUFJAVOOONJE-UHFFFAOYSA-N beta-cariophyllene Natural products C1CC(C)=CCCC(=C)C2CC(C)(C)C21 NPNUFJAVOOONJE-UHFFFAOYSA-N 0.000 description 1
UPVZPMJSRSWJHQ-XIQJJJERSA-N beta-copaene Chemical compound C1CC(=C)C2[C@@]3(C)CC[C@@H](C(C)C)[C@H]2[C@@H]31 UPVZPMJSRSWJHQ-XIQJJJERSA-N 0.000 description 1
WHGYBXFWUBPSRW-FOUAGVGXSA-N beta-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO WHGYBXFWUBPSRW-FOUAGVGXSA-N 0.000 description 1
235000011175 beta-cyclodextrine Nutrition 0.000 description 1
YOVSPTNQHMDJAG-UHFFFAOYSA-N beta-helmiscapene Natural products C1CCC(=C)C2CC(C(=C)C)CCC21C YOVSPTNQHMDJAG-UHFFFAOYSA-N 0.000 description 1
LCOSCMLXPAQCLQ-UHFFFAOYSA-N beta-himachalene Chemical compound C1CC(C)=CC2C1=C(C)CCCC2(C)C LCOSCMLXPAQCLQ-UHFFFAOYSA-N 0.000 description 1
RGMFHVSYUMRAIL-UHFFFAOYSA-N beta-ionone epoxide Natural products CC1OC1CC2=C(C)CCCC2(C)C RGMFHVSYUMRAIL-UHFFFAOYSA-N 0.000 description 1
NOPLRNXKHZRXHT-FBXUGWQNSA-N beta-sinensal Natural products O=C/C(=C\CC/C(=C\CCC(C=C)=C)/C)/C NOPLRNXKHZRXHT-FBXUGWQNSA-N 0.000 description 1
229960004853 betadex Drugs 0.000 description 1
229950011260 betanaphthol Drugs 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
229930003493 bisabolene Natural products 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229930006711 bornane-2,3-dione Natural products 0.000 description 1
YXXPNGIZHZHBTQ-UHFFFAOYSA-N butan-2-ol Chemical compound CC[C](C)O YXXPNGIZHZHBTQ-UHFFFAOYSA-N 0.000 description 1
FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 1
ULBTUVJTXULMLP-UHFFFAOYSA-N butyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCC ULBTUVJTXULMLP-UHFFFAOYSA-N 0.000 description 1
229940095259 butylated hydroxytoluene Drugs 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229910000281 calcium bentonite Inorganic materials 0.000 description 1
ZYPYEBYNXWUCEA-UHFFFAOYSA-N camphenilone Natural products C1CC2C(=O)C(C)(C)C1C2 ZYPYEBYNXWUCEA-UHFFFAOYSA-N 0.000 description 1
229930008380 camphor Natural products 0.000 description 1
229960000846 camphor Drugs 0.000 description 1
150000001734 carboxylic acid salts Chemical class 0.000 description 1
239000012876 carrier material Substances 0.000 description 1
235000007746 carvacrol Nutrition 0.000 description 1
WPGPCDVQHXOMQP-UHFFFAOYSA-N carvotanacetone Natural products CC(C)C1CC=C(C)C(=O)C1 WPGPCDVQHXOMQP-UHFFFAOYSA-N 0.000 description 1
NPNUFJAVOOONJE-UONOGXRCSA-N caryophyllene Natural products C1CC(C)=CCCC(=C)[C@@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-UONOGXRCSA-N 0.000 description 1
RSYBQKUNBFFNDO-UHFFFAOYSA-N caryophyllene oxide Natural products CC1(C)CC2C(=C)CCC3OC3(C)CCC12C RSYBQKUNBFFNDO-UHFFFAOYSA-N 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
229960000541 cetyl alcohol Drugs 0.000 description 1
230000008859 change Effects 0.000 description 1
229960005443 chloroxylenol Drugs 0.000 description 1
229960005233 cineole Drugs 0.000 description 1
RFFOTVCVTJUTAD-UHFFFAOYSA-N cineole Natural products C1CC2(C)CCC1(C(C)C)O2 RFFOTVCVTJUTAD-UHFFFAOYSA-N 0.000 description 1
229940114081 cinnamate Drugs 0.000 description 1
CCRCUPLGCSFEDV-UHFFFAOYSA-N cinnamic acid methyl ester Natural products COC(=O)C=CC1=CC=CC=C1 CCRCUPLGCSFEDV-UHFFFAOYSA-N 0.000 description 1
LGTLDEUQCOJGFP-WAYWQWQTSA-N cis-3-Hexenyl propanoate Chemical compound CC\C=C/CCOC(=O)CC LGTLDEUQCOJGFP-WAYWQWQTSA-N 0.000 description 1
AIQLNKITFBJPFO-WAYWQWQTSA-N cis-3-hexenyl isovalerate Chemical compound CC\C=C/CCOC(=O)CC(C)C AIQLNKITFBJPFO-WAYWQWQTSA-N 0.000 description 1
ZCHOPXVYTWUHDS-UHFFFAOYSA-N cis-3-hexenyl n-butyrate Natural products CCCC(=O)OCCC=CCC ZCHOPXVYTWUHDS-UHFFFAOYSA-N 0.000 description 1
GFJIQNADMLPFOW-UHFFFAOYSA-N cis-Elemol Natural products CC(=C)C1CC(C(C)(C)O)CCC1(C)C=C GFJIQNADMLPFOW-UHFFFAOYSA-N 0.000 description 1
BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 description 1
235000020971 citrus fruits Nutrition 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
239000003086 colorant Substances 0.000 description 1
239000012612 commercial material Substances 0.000 description 1
230000000295 complement effect Effects 0.000 description 1
238000006482 condensation reaction Methods 0.000 description 1
235000005687 corn oil Nutrition 0.000 description 1
239000002285 corn oil Substances 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
235000012343 cottonseed oil Nutrition 0.000 description 1
239000002385 cottonseed oil Substances 0.000 description 1
VUSWCWPCANWBFG-UHFFFAOYSA-N cyclohex-3-ene-1-carboxylic acid Chemical compound OC(=O)C1CCC=CC1 VUSWCWPCANWBFG-UHFFFAOYSA-N 0.000 description 1
ABRIMXGLNHCLIP-UHFFFAOYSA-N cyclohexadec-5-en-1-one Chemical compound O=C1CCCCCCCCCCC=CCCC1 ABRIMXGLNHCLIP-UHFFFAOYSA-N 0.000 description 1
CIISBNCSMVCNIP-UHFFFAOYSA-N cyclopentane-1,2-dione Chemical compound O=C1CCCC1=O CIISBNCSMVCNIP-UHFFFAOYSA-N 0.000 description 1
XOVJAYNMQDTIJD-UHFFFAOYSA-N cyclopentobarbital Chemical compound C1CC=CC1C1(CC=C)C(=O)NC(=O)NC1=O XOVJAYNMQDTIJD-UHFFFAOYSA-N 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
YMGUBTXCNDTFJI-UHFFFAOYSA-M cyclopropanecarboxylate Chemical compound [O-]C(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-M 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
230000018044 dehydration Effects 0.000 description 1
238000006297 dehydration reaction Methods 0.000 description 1
YHAJBLWYOIUHHM-UHFFFAOYSA-N delta-guaiene Natural products C1CC(C(C)=C)CC2C(C)CCC2=C1C YHAJBLWYOIUHHM-UHFFFAOYSA-N 0.000 description 1
230000008021 deposition Effects 0.000 description 1
125000005265 dialkylamine group Chemical group 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
JHJCHCSUEGPIGE-LBPRGKRZSA-N dihydro-α-ionone Chemical compound CC(=O)CC[C@H]1C(C)=CCCC1(C)C JHJCHCSUEGPIGE-LBPRGKRZSA-N 0.000 description 1
229930007024 dihydrocarveol Natural products 0.000 description 1
DMSHWWDRAYHEBS-UHFFFAOYSA-N dihydrocoumarin Natural products C1CC(=O)OC2=C1C=C(OC)C(OC)=C2 DMSHWWDRAYHEBS-UHFFFAOYSA-N 0.000 description 1
POSWICCRDBKBMH-UHFFFAOYSA-N dihydroisophorone Natural products CC1CC(=O)CC(C)(C)C1 POSWICCRDBKBMH-UHFFFAOYSA-N 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
UAKOZKUVZRMOFN-JDVCJPALSA-M dimethyl-bis[(z)-octadec-9-enyl]azanium;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCC[N+](C)(C)CCCCCCCC\C=C/CCCCCCCC UAKOZKUVZRMOFN-JDVCJPALSA-M 0.000 description 1
ROSDSFDQCJNGOL-UHFFFAOYSA-O dimethylaminium Chemical compound C[NH2+]C ROSDSFDQCJNGOL-UHFFFAOYSA-O 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
238000004821 distillation Methods 0.000 description 1
JLPUXFOGCDVKGO-UHFFFAOYSA-N dl-geosmin Natural products C1CCCC2(O)C(C)CCCC21C JLPUXFOGCDVKGO-UHFFFAOYSA-N 0.000 description 1
KFEVDPWXEVUUMW-UHFFFAOYSA-N docosanoic acid Natural products CCCCCCCCCCCCCCCCCCCCCC(=O)OCCC1=CC=C(O)C=C1 KFEVDPWXEVUUMW-UHFFFAOYSA-N 0.000 description 1
PSFYZDSSGMTRJE-UHFFFAOYSA-N dodecanoic acid;heptatriacontan-19-amine Chemical compound CCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCCC(N)CCCCCCCCCCCCCCCCCC PSFYZDSSGMTRJE-UHFFFAOYSA-N 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000000694 effects Effects 0.000 description 1
IEICDHBPEPUHOB-UHFFFAOYSA-N ent-beta-selinene Natural products C1CCC(=C)C2CC(C(C)C)CCC21C IEICDHBPEPUHOB-UHFFFAOYSA-N 0.000 description 1
UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
229940009714 erythritol Drugs 0.000 description 1
235000019414 erythritol Nutrition 0.000 description 1
FARYTWBWLZAXNK-WAYWQWQTSA-N ethyl (z)-3-(methylamino)but-2-enoate Chemical compound CCOC(=O)\C=C(\C)NC FARYTWBWLZAXNK-WAYWQWQTSA-N 0.000 description 1
KRCQDQXKPOKJOE-UHFFFAOYSA-N ethyl deca-2,4,7-trienoate Chemical compound CCOC(=O)C=CC=CCC=CCC KRCQDQXKPOKJOE-UHFFFAOYSA-N 0.000 description 1
229940093476 ethylene glycol Drugs 0.000 description 1
BAVONGHXFVOKBV-UHFFFAOYSA-N exo-carveol Natural products CC(=C)C1CC=C(C)C(O)C1 BAVONGHXFVOKBV-UHFFFAOYSA-N 0.000 description 1
125000005313 fatty acid group Chemical group 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
150000002192 fatty aldehydes Chemical class 0.000 description 1
150000002193 fatty amides Chemical class 0.000 description 1
239000010685 fatty oil Substances 0.000 description 1
230000002550 fecal effect Effects 0.000 description 1
238000000855 fermentation Methods 0.000 description 1
230000004151 fermentation Effects 0.000 description 1
239000000834 fixative Substances 0.000 description 1
239000000796 flavoring agent Substances 0.000 description 1
235000019634 flavors Nutrition 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000012634 fragment Substances 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
229930014097 furanoid Natural products 0.000 description 1
OALYTRUKMRCXNH-QMMMGPOBSA-N gamma-Nonalactone Natural products CCCCC[C@H]1CCC(=O)O1 OALYTRUKMRCXNH-QMMMGPOBSA-N 0.000 description 1
LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
RVOXATXFYDNXRE-UHFFFAOYSA-N gamma-elemene Natural products CC(=C1CCC(C)(C(C1)C(=C)C)C(=C)C)C RVOXATXFYDNXRE-UHFFFAOYSA-N 0.000 description 1
229930007090 gamma-ionone Natural products 0.000 description 1
229940020436 gamma-undecalactone Drugs 0.000 description 1
238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
235000003869 genetically modified organism Nutrition 0.000 description 1
229930001467 geosmin Natural products 0.000 description 1
CCCXGQLQJHWTLZ-UHFFFAOYSA-N geranyl linalool Natural products CC(=CCCC(=CCCCC(C)(O)CCC=C(C)C)C)C CCCXGQLQJHWTLZ-UHFFFAOYSA-N 0.000 description 1
YYBMOGCOPQVSLQ-UHFFFAOYSA-N geranyl octanoate Natural products CCCCCCCC(=O)OCC=C(C)CCC=C(C)C YYBMOGCOPQVSLQ-UHFFFAOYSA-N 0.000 description 1
UXAIJXIHZDZMSK-VBKFSLOCSA-N geranyl phenylacetate Chemical compound CC(C)=CCC\C(C)=C/COC(=O)CC1=CC=CC=C1 UXAIJXIHZDZMSK-VBKFSLOCSA-N 0.000 description 1
OJIGFVZZEVQUNV-UHFFFAOYSA-N germacrene D Natural products CC(C)C1CCC=C(/C)CCC(=C)C=C1 OJIGFVZZEVQUNV-UHFFFAOYSA-N 0.000 description 1
230000002070 germicidal effect Effects 0.000 description 1
230000009477 glass transition Effects 0.000 description 1
239000008103 glucose Substances 0.000 description 1
239000004519 grease Substances 0.000 description 1
TWVJWDMOZJXUID-QJPTWQEYSA-N guaiol Natural products OC(C)(C)[C@H]1CC=2[C@H](C)CCC=2[C@@H](C)CC1 TWVJWDMOZJXUID-QJPTWQEYSA-N 0.000 description 1
239000000665 guar gum Substances 0.000 description 1
229960002154 guar gum Drugs 0.000 description 1
235000010417 guar gum Nutrition 0.000 description 1
235000019382 gum benzoic Nutrition 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
CBAGROYOJMZIRK-UHFFFAOYSA-N hepta-1,6-dien-3-one Chemical compound C=CCCC(=O)C=C CBAGROYOJMZIRK-UHFFFAOYSA-N 0.000 description 1
NORNNWWOOVVGCT-UHFFFAOYSA-N heptatriacontan-19-amine;hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCCC(N)CCCCCCCCCCCCCCCCCC NORNNWWOOVVGCT-UHFFFAOYSA-N 0.000 description 1
KNGVHBHJHHSSQG-UHFFFAOYSA-N heptatriacontan-19-amine;tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCCC(N)CCCCCCCCCCCCCCCCCC KNGVHBHJHHSSQG-UHFFFAOYSA-N 0.000 description 1
JHGVLAHJJNKSAW-UHFFFAOYSA-N herniarin Natural products C1CC(=O)OC2=CC(OC)=CC=C21 JHGVLAHJJNKSAW-UHFFFAOYSA-N 0.000 description 1
XPFTVTFOOTVHIA-UHFFFAOYSA-N hex-3-enyl pentanoate Chemical compound CCCCC(=O)OCCC=CCC XPFTVTFOOTVHIA-UHFFFAOYSA-N 0.000 description 1
DDQDBZUGVZGFKB-UHFFFAOYSA-N hexahydro-4,7-methanoinden-6-yl propionate Chemical compound C1CCC2C(C3)CC(OC(=O)CC)C3=C21 DDQDBZUGVZGFKB-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
239000008172 hydrogenated vegetable oil Substances 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
238000009884 interesterification Methods 0.000 description 1
229940078565 isoamyl laurate Drugs 0.000 description 1
DIICMQCJAQLQPI-UHFFFAOYSA-N isobornyl propionate Natural products CCC(=O)C1CC2CCC1(C)C2(C)C DIICMQCJAQLQPI-UHFFFAOYSA-N 0.000 description 1
WYXXLXHHWYNKJF-UHFFFAOYSA-N isocarvacrol Natural products CC(C)C1=CC=C(O)C(C)=C1 WYXXLXHHWYNKJF-UHFFFAOYSA-N 0.000 description 1
HWXIVVHIYFTBBZ-UHFFFAOYSA-N isochromene Chemical compound C1=CC=C2[CH]OC=CC2=C1 HWXIVVHIYFTBBZ-UHFFFAOYSA-N 0.000 description 1
GAIBLDCXCZKKJE-UHFFFAOYSA-N isogermacrene D Natural products CC(C)C1CCC(C)=CCCC(=C)C=C1 GAIBLDCXCZKKJE-UHFFFAOYSA-N 0.000 description 1
238000006317 isomerization reaction Methods 0.000 description 1
229940075495 isopropyl palmitate Drugs 0.000 description 1
229940095045 isopulegol Drugs 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
125000000400 lauroyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229940087305 limonene Drugs 0.000 description 1
235000020778 linoleic acid Nutrition 0.000 description 1
OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
210000004072 lung Anatomy 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
230000000873 masking effect Effects 0.000 description 1
HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
TWXDDNPPQUTEOV-FVGYRXGTSA-N methamphetamine hydrochloride Chemical compound Cl.CN[C@@H](C)CC1=CC=CC=C1 TWXDDNPPQUTEOV-FVGYRXGTSA-N 0.000 description 1
KDSJAOIHFZMUNK-SDNWHVSQSA-N methyl 2-[[(e)-(2,4-dimethylcyclohex-3-en-1-ylidene)methyl]amino]benzoate Chemical compound COC(=O)C1=CC=CC=C1N\C=C/1C(C)C=C(C)CC\1 KDSJAOIHFZMUNK-SDNWHVSQSA-N 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
AKDNDOBRFDICST-UHFFFAOYSA-N methylazanium;methyl sulfate Chemical compound [NH3+]C.COS([O-])(=O)=O AKDNDOBRFDICST-UHFFFAOYSA-N 0.000 description 1
229940116837 methyleugenol Drugs 0.000 description 1
PRHTXAOWJQTLBO-UHFFFAOYSA-N methyleugenol Natural products COC1=CC=C(C(C)=C)C=C1OC PRHTXAOWJQTLBO-UHFFFAOYSA-N 0.000 description 1
239000003094 microcapsule Substances 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
239000008267 milk Substances 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
229940067137 musk ketone Drugs 0.000 description 1
YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 1
ITFGZZGYXVHOOU-UHFFFAOYSA-N n,n-dimethylmethanamine;methyl hydrogen sulfate Chemical compound C[NH+](C)C.COS([O-])(=O)=O ITFGZZGYXVHOOU-UHFFFAOYSA-N 0.000 description 1
ZXALKJAAQSZAQQ-UHFFFAOYSA-N n,n-dimethyloctadecan-1-amine;octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCCN(C)C ZXALKJAAQSZAQQ-UHFFFAOYSA-N 0.000 description 1
HPHYXUHORODDLS-UHFFFAOYSA-N n,n-dimethyloctadecan-1-amine;tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCCN(C)C HPHYXUHORODDLS-UHFFFAOYSA-N 0.000 description 1
SFBHPFQSSDCYSL-UHFFFAOYSA-N n,n-dimethyltetradecan-1-amine Chemical compound CCCCCCCCCCCCCCN(C)C SFBHPFQSSDCYSL-UHFFFAOYSA-N 0.000 description 1
UWHRNIXHZAWBMF-UHFFFAOYSA-N n-dodecyl-n-methyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)CCCCCCCCCCCC UWHRNIXHZAWBMF-UHFFFAOYSA-N 0.000 description 1
VFLWKHBYVIUAMP-UHFFFAOYSA-N n-methyl-n-octadecyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCN(C)CCCCCCCCCCCCCCCCCC VFLWKHBYVIUAMP-UHFFFAOYSA-N 0.000 description 1
QWERMLCFPMTLTG-UHFFFAOYSA-N n-methyltetradecan-1-amine Chemical compound CCCCCCCCCCCCCCNC QWERMLCFPMTLTG-UHFFFAOYSA-N 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
ZYTMANIQRDEHIO-UHFFFAOYSA-N neo-Isopulegol Natural products CC1CCC(C(C)=C)C(O)C1 ZYTMANIQRDEHIO-UHFFFAOYSA-N 0.000 description 1
WASNIKZYIWZQIP-AWEZNQCLSA-N nerolidol Natural products CC(=CCCC(=CCC[C@@H](O)C=C)C)C WASNIKZYIWZQIP-AWEZNQCLSA-N 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
DSOXXQLCMAEPEZ-UHFFFAOYSA-N nona-2,6-dienenitrile Chemical compound CCC=CCCC=CC#N DSOXXQLCMAEPEZ-UHFFFAOYSA-N 0.000 description 1
PICGPEBVZGCYBV-UHFFFAOYSA-N nona-3,6-dien-1-ol Chemical compound CCC=CCC=CCCO PICGPEBVZGCYBV-UHFFFAOYSA-N 0.000 description 1
ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 description 1
BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 1
150000007823 ocimene derivatives Chemical class 0.000 description 1
CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 description 1
229960002446 octanoic acid Drugs 0.000 description 1
229940049964 oleate Drugs 0.000 description 1
125000002811 oleoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
125000005375 organosiloxane group Chemical group 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
ATYBXHSAIOKLMG-UHFFFAOYSA-N oxepin Chemical compound O1C=CC=CC=C1 ATYBXHSAIOKLMG-UHFFFAOYSA-N 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
150000002923 oximes Chemical class 0.000 description 1
229960001173 oxybenzone Drugs 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
XJWZDXFFNOMMTD-JTQLQIEISA-N p-Menth-3-en-1-ol Natural products CC(C)C1=CC[C@](C)(O)CC1 XJWZDXFFNOMMTD-JTQLQIEISA-N 0.000 description 1
125000000552 p-cresyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1O*)C([H])([H])[H] 0.000 description 1
239000003346 palm kernel oil Substances 0.000 description 1
235000019865 palm kernel oil Nutrition 0.000 description 1
125000001312 palmitoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000312 peanut oil Substances 0.000 description 1
229940059574 pentaerithrityl Drugs 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
235000005693 perillyl alcohol Nutrition 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
LCPDWSOZIOUXRV-UHFFFAOYSA-N phenoxyacetic acid Chemical compound OC(=O)COC1=CC=CC=C1 LCPDWSOZIOUXRV-UHFFFAOYSA-N 0.000 description 1
229960005323 phenoxyethanol Drugs 0.000 description 1
XOKSLPVRUOBDEW-UHFFFAOYSA-N pinane of uncertain configuration Natural products CC1CCC2C(C)(C)C1C2 XOKSLPVRUOBDEW-UHFFFAOYSA-N 0.000 description 1
229930006721 pinocarveol Natural products 0.000 description 1
IUGYQRQAERSCNH-UHFFFAOYSA-M pivalate Chemical compound CC(C)(C)C([O-])=O IUGYQRQAERSCNH-UHFFFAOYSA-M 0.000 description 1
JAMNHZBIQDNHMM-UHFFFAOYSA-N pivalonitrile Chemical compound CC(C)(C)C#N JAMNHZBIQDNHMM-UHFFFAOYSA-N 0.000 description 1
238000004987 plasma desorption mass spectroscopy Methods 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920000136 polysorbate Polymers 0.000 description 1
235000020777 polyunsaturated fatty acids Nutrition 0.000 description 1
239000011591 potassium Substances 0.000 description 1
230000003389 potentiating effect Effects 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
BNXQSAVKKDIKRX-UHFFFAOYSA-N propan-2-yl bicyclo[2.2.1]hept-2-ene-5-carboxylate Chemical compound C1C2C(C(=O)OC(C)C)CC1C=C2 BNXQSAVKKDIKRX-UHFFFAOYSA-N 0.000 description 1
QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 1
229940080818 propionamide Drugs 0.000 description 1
ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 1
238000000746 purification Methods 0.000 description 1
238000005956 quaternization reaction Methods 0.000 description 1
MXDMETWAEGIFOE-UHFFFAOYSA-N rac-delta-elemene Natural products CC(C)C1=CC(C(C)=C)C(C)(C=C)CC1 MXDMETWAEGIFOE-UHFFFAOYSA-N 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000011160 research Methods 0.000 description 1
239000013557 residual solvent Substances 0.000 description 1
230000004044 response Effects 0.000 description 1
239000008165 rice bran oil Substances 0.000 description 1
235000005713 safflower oil Nutrition 0.000 description 1
239000003813 safflower oil Substances 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
230000008786 sensory perception of smell Effects 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
229920002050 silicone resin Polymers 0.000 description 1
229940074386 skatole Drugs 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000000264 sodium ferrocyanide Substances 0.000 description 1
KWVISVAMQJWJSZ-VKROHFNGSA-N solasodine Chemical compound O([C@@H]1[C@@H]([C@]2(CC[C@@H]3[C@@]4(C)CC[C@H](O)CC4=CC[C@H]3[C@@H]2C1)C)[C@@H]1C)[C@]11CC[C@@H](C)CN1 KWVISVAMQJWJSZ-VKROHFNGSA-N 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
229940035044 sorbitan monolaurate Drugs 0.000 description 1
239000001593 sorbitan monooleate Substances 0.000 description 1
235000011069 sorbitan monooleate Nutrition 0.000 description 1
229940035049 sorbitan monooleate Drugs 0.000 description 1
239000001570 sorbitan monopalmitate Substances 0.000 description 1
235000011071 sorbitan monopalmitate Nutrition 0.000 description 1
229940031953 sorbitan monopalmitate Drugs 0.000 description 1
229950003429 sorbitan palmitate Drugs 0.000 description 1
229950011392 sorbitan stearate Drugs 0.000 description 1
239000001589 sorbitan tristearate Substances 0.000 description 1
235000011078 sorbitan tristearate Nutrition 0.000 description 1
229960004129 sorbitan tristearate Drugs 0.000 description 1
KPBWTXWXUKLAPR-UHFFFAOYSA-N spiro[1,3-dioxolane-2,5'-tricyclo[6.2.1.01,6]undeca-3,6,9-triene] Chemical compound O1CCOC21C1=CC(C=C3)CC31CC=C2 KPBWTXWXUKLAPR-UHFFFAOYSA-N 0.000 description 1
CTDQAGUNKPRERK-UHFFFAOYSA-N spirodecane Chemical compound C1CCCC21CCCCC2 CTDQAGUNKPRERK-UHFFFAOYSA-N 0.000 description 1
229930194661 spirolide Natural products 0.000 description 1
238000007655 standard test method Methods 0.000 description 1
230000003068 static effect Effects 0.000 description 1
125000003696 stearoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000000185 sucrose group Chemical group 0.000 description 1
239000002600 sunflower oil Substances 0.000 description 1
239000003784 tall oil Substances 0.000 description 1
229940116411 terpineol Drugs 0.000 description 1
DKGAVHZHDRPRBM-UHFFFAOYSA-N tert-butyl alcohol Substances CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
XTVMZZBLCLWBPM-UHFFFAOYSA-N tert-butylcyclohexane Chemical compound CC(C)(C)C1CCCCC1 XTVMZZBLCLWBPM-UHFFFAOYSA-N 0.000 description 1
QZZGJDVWLFXDLK-UHFFFAOYSA-N tetracosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC(O)=O QZZGJDVWLFXDLK-UHFFFAOYSA-N 0.000 description 1
TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical class CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
239000004753 textile Substances 0.000 description 1
229960000790 thymol Drugs 0.000 description 1
UIERETOOQGIECD-ONEGZZNKSA-N tiglic acid Chemical compound C\C=C(/C)C(O)=O UIERETOOQGIECD-ONEGZZNKSA-N 0.000 description 1
GCRTVIUGJCJVDD-IUCAKERBSA-N trans-Dihydrocarvone Chemical compound CC(C)[C@H]1CC[C@H](C)C(=O)C1 GCRTVIUGJCJVDD-IUCAKERBSA-N 0.000 description 1
NPNUFJAVOOONJE-ZIAGYGMSSA-N trans-caryophyllene Natural products C1CC(C)=CCCC(=C)[C@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-ZIAGYGMSSA-N 0.000 description 1
WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical compound [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
WBYWAXJHAXSJNI-VOTSOKGWSA-N trans-cinnamic acid Chemical compound OC(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-N 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
125000005270 trialkylamine group Chemical group 0.000 description 1
WKSPQBFDRTUGEF-UHFFFAOYSA-N tridec-2-enenitrile Chemical compound CCCCCCCCCCC=CC#N WKSPQBFDRTUGEF-UHFFFAOYSA-N 0.000 description 1
DBWSGRFEGVADLQ-UHFFFAOYSA-N trideca-3,12-dienenitrile Chemical compound C=CCCCCCCCC=CCC#N DBWSGRFEGVADLQ-UHFFFAOYSA-N 0.000 description 1
229940087291 tridecyl alcohol Drugs 0.000 description 1
SWZDQOUHBYYPJD-UHFFFAOYSA-N tridodecylamine Chemical compound CCCCCCCCCCCCN(CCCCCCCCCCCC)CCCCCCCCCCCC SWZDQOUHBYYPJD-UHFFFAOYSA-N 0.000 description 1
239000001069 triethyl citrate Substances 0.000 description 1
VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 1
235000013769 triethyl citrate Nutrition 0.000 description 1
PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
229940117972 triolein Drugs 0.000 description 1
239000002383 tung oil Substances 0.000 description 1
WENNKWXPAWNIOO-UHFFFAOYSA-N undecan-5-one Chemical compound CCCCCCC(=O)CCCC WENNKWXPAWNIOO-UHFFFAOYSA-N 0.000 description 1
125000004417 unsaturated alkyl group Chemical group 0.000 description 1
150000003673 urethanes Chemical class 0.000 description 1
210000002700 urine Anatomy 0.000 description 1
WCTNXGFHEZQHDR-UHFFFAOYSA-N valencene Natural products C1CC(C)(C)C2(C)CC(C(=C)C)CCC2=C1 WCTNXGFHEZQHDR-UHFFFAOYSA-N 0.000 description 1
BALAUIYKESNHDW-UHFFFAOYSA-N verdyl propionate Chemical compound C1CC2C3C(OC(=O)CC)C=CC3C1C2 BALAUIYKESNHDW-UHFFFAOYSA-N 0.000 description 1
238000005303 weighing Methods 0.000 description 1
239000000811 xylitol Substances 0.000 description 1
235000010447 xylitol Nutrition 0.000 description 1
HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
229960002675 xylitol Drugs 0.000 description 1
229930000038 α-guaiene Natural products 0.000 description 1
USMNOWBWPHYOEA-MRTMQBJTSA-N α-thujone Chemical compound O=C([C@@H]1C)C[C@@]2(C(C)C)[C@@H]1C2 USMNOWBWPHYOEA-MRTMQBJTSA-N 0.000 description 1
229930000053 β-bisabolol Natural products 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/01—Deodorant compositions
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F30/00—Computer-aided design [CAD]
- G06F30/20—Design optimisation, verification or simulation
- G06F30/23—Design optimisation, verification or simulation using finite element methods [FEM] or finite difference methods [FDM]
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/11—Encapsulated compositions
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/31—Hydrocarbons
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/361—Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/368—Carboxylic acids; Salts or anhydrides thereof with carboxyl groups directly bound to carbon atoms of aromatic rings
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4926—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4966—Triazines or their condensed derivatives
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
- A61K8/498—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom having 6-membered rings or their condensed derivatives, e.g. coumarin
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/58—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/731—Cellulose; Quaternized cellulose derivatives
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/20—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing organic materials
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
- A61L15/28—Polysaccharides or their derivatives
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
- A61L15/46—Deodorants or malodour counteractants, e.g. to inhibit the formation of ammonia or bacteria
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/01—Deodorant compositions
- A61L9/012—Deodorant compositions characterised by being in a special form, e.g. gels, emulsions
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/015—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone
- A61L9/04—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating
- A61L9/12—Apparatus, e.g. holders, therefor
- A61L9/122—Apparatus, e.g. holders, therefor comprising a fan
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/015—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone
- A61L9/04—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating
- A61L9/12—Apparatus, e.g. holders, therefor
- A61L9/127—Apparatus, e.g. holders, therefor comprising a wick
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/14—Disinfection, sterilisation or deodorisation of air using sprayed or atomised substances including air-liquid contact processes
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
- B01J20/24—Naturally occurring macromolecular compounds, e.g. humic acids or their derivatives
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0007—Aliphatic compounds
- C11B9/0015—Aliphatic compounds containing oxygen as the only heteroatom
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0007—Aliphatic compounds
- C11B9/0015—Aliphatic compounds containing oxygen as the only heteroatom
- C11B9/0019—Aliphatic compounds containing oxygen as the only heteroatom carbocylic acids; Salts or esters thereof
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
- C11B9/003—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing less than six carbon atoms
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
- C11B9/0034—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing six carbon atoms
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
- C11B9/0038—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing more than six carbon atoms
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0042—Essential oils; Perfumes compounds containing condensed hydrocarbon rings
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0042—Essential oils; Perfumes compounds containing condensed hydrocarbon rings
- C11B9/0046—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings
- C11B9/0049—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings the condensed rings sharing two common C atoms
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0042—Essential oils; Perfumes compounds containing condensed hydrocarbon rings
- C11B9/0046—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings
- C11B9/0049—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings the condensed rings sharing two common C atoms
- C11B9/0053—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings the condensed rings sharing two common C atoms both rings being six-membered
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0061—Essential oils; Perfumes compounds containing a six-membered aromatic ring not condensed with another ring
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0069—Heterocyclic compounds
- C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
- C11B9/0076—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing less than six atoms
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0069—Heterocyclic compounds
- C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
- C11B9/008—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing six atoms
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0069—Heterocyclic compounds
- C11B9/0092—Heterocyclic compounds containing only N as heteroatom
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0043—For use with aerosol devices
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C11D17/042—Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C11D17/047—Arrangements specially adapted for dry cleaning or laundry dryer related applications
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0068—Deodorant compositions
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/18—Hydrocarbons
- C11D3/184—Hydrocarbons unsaturated
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2006—Monohydric alcohols
- C11D3/2034—Monohydric alcohols aromatic
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2068—Ethers
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2072—Aldehydes-ketones
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2079—Monocarboxylic acids-salts thereof
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2093—Esters; Carbonates
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2096—Heterocyclic compounds
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/30—Amines; Substituted amines ; Quaternized amines
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/43—Solvents
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
- C11D3/502—Protected perfumes
- C11D3/505—Protected perfumes encapsulated or adsorbed on a carrier, e.g. zeolite or clay
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06B—TREATING TEXTILE MATERIALS USING LIQUIDS, GASES OR VAPOURS
- D06B1/00—Applying liquids, gases or vapours onto textile materials to effect treatment, e.g. washing, dyeing, bleaching, sizing or impregnating
- D06B1/02—Applying liquids, gases or vapours onto textile materials to effect treatment, e.g. washing, dyeing, bleaching, sizing or impregnating by spraying or projecting
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F17/00—Digital computing or data processing equipment or methods, specially adapted for specific functions
- G06F17/10—Complex mathematical operations
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F17/00—Digital computing or data processing equipment or methods, specially adapted for specific functions
- G06F17/10—Complex mathematical operations
- G06F17/11—Complex mathematical operations for solving equations, e.g. nonlinear equations, general mathematical optimization problems
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06Q—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES, NOT OTHERWISE PROVIDED FOR
- G06Q99/00—Subject matter not provided for in other groups of this subclass
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16C—COMPUTATIONAL CHEMISTRY; CHEMOINFORMATICS; COMPUTATIONAL MATERIALS SCIENCE
- G16C10/00—Computational theoretical chemistry, i.e. ICT specially adapted for theoretical aspects of quantum chemistry, molecular mechanics, molecular dynamics or the like
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16C—COMPUTATIONAL CHEMISTRY; CHEMOINFORMATICS; COMPUTATIONAL MATERIALS SCIENCE
- G16C20/00—Chemoinformatics, i.e. ICT specially adapted for the handling of physicochemical or structural data of chemical particles, elements, compounds or mixtures
- G16C20/40—Searching chemical structures or physicochemical data
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/56—Compounds, absorbed onto or entrapped into a solid carrier, e.g. encapsulated perfumes, inclusion compounds, sustained release forms
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/592—Mixtures of compounds complementing their respective functions
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/592—Mixtures of compounds complementing their respective functions
- A61K2800/5922—At least two compounds being classified in the same subclass of A61K8/18
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
- A61L2/18—Liquid substances or solutions comprising solids or dissolved gases
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2209/00—Aspects relating to disinfection, sterilisation or deodorisation of air
- A61L2209/10—Apparatus features
- A61L2209/13—Dispensing or storing means for active compounds
- A61L2209/133—Replaceable cartridges, refills
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2209/00—Aspects relating to disinfection, sterilisation or deodorisation of air
- A61L2209/10—Apparatus features
- A61L2209/13—Dispensing or storing means for active compounds
- A61L2209/134—Distributing means, e.g. baffles, valves, manifolds, nozzles
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2209/00—Aspects relating to disinfection, sterilisation or deodorisation of air
- A61L2209/20—Method-related aspects
- A61L2209/21—Use of chemical compounds for treating air or the like
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/60—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a special physical form
- A61L2300/62—Encapsulated active agents, e.g. emulsified droplets
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/015—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone
- A61L9/02—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air by heating or combustion
- A61L9/03—Apparatus therefor
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/12—Soft surfaces, e.g. textile

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
General Health & Medical Sciences (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Animal Behavior & Ethology (AREA)
Epidemiology (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Birds (AREA)
Emergency Medicine (AREA)
Theoretical Computer Science (AREA)
Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Dermatology (AREA)
Hematology (AREA)
Materials Engineering (AREA)
Computing Systems (AREA)
Mathematical Physics (AREA)
Data Mining & Analysis (AREA)
Dispersion Chemistry (AREA)
Bioinformatics & Cheminformatics (AREA)
Crystallography & Structural Chemistry (AREA)
Bioinformatics & Computational Biology (AREA)
Mathematical Optimization (AREA)
Computational Mathematics (AREA)
Pure & Applied Mathematics (AREA)
Mathematical Analysis (AREA)
General Engineering & Computer Science (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
General Business, Economics & Management (AREA)
Business, Economics & Management (AREA)
Databases & Information Systems (AREA)
Algebra (AREA)
Software Systems (AREA)

CA2959695A 2014-09-26 2015-09-25 Substrats contenant des compositions reduisant les mauvaises odeurs Abandoned CA2959695A1 (fr)

Applications Claiming Priority (5)

Application Number	Priority Date	Filing Date	Title
US201462055844P	2014-09-26	2014-09-26
US62/055,844		2014-09-26
US201562143862P	2015-04-07	2015-04-07
US62/143,862		2015-04-07
PCT/US2015/052119 WO2016049404A1 (fr)	2014-09-26	2015-09-25	Substrats contenant des compositions réduisant les mauvaises odeurs

Publications (1)

Publication Number	Publication Date
CA2959695A1 true CA2959695A1 (fr)	2016-03-31

Family

ID=54256860

Family Applications (9)

Application Number	Title	Priority Date	Filing Date
CA2959432A Abandoned CA2959432A1 (fr)	2014-09-26	2015-09-25	Compositions de reduction des mauvaises odeurs
CA2960394A Pending CA2960394A1 (fr)	2014-09-26	2015-09-25	Compositions rafraichissantes et dispositifs comprenant celles-ci
CA2959697A Pending CA2959697A1 (fr)	2014-09-26	2015-09-25	Systemes d'administration comprenant des compositions de reduction des mauvaises odeurs
CA2960390A Pending CA2960390A1 (fr)	2014-09-26	2015-09-25	Compositions rafraichissantes et dispositifs les comprenant
CA2959546A Abandoned CA2959546A1 (fr)	2014-09-26	2015-09-25	Compositions de nettoyage et/ou de traitement comportant des compositions de reduction de mauvaises odeurs
CA2959555A Pending CA2959555A1 (fr)	2014-09-26	2015-09-25	Procede de fabrication d'articles parfumes
CA2959695A Abandoned CA2959695A1 (fr)	2014-09-26	2015-09-25	Substrats contenant des compositions reduisant les mauvaises odeurs
CA2959434A Active CA2959434C (fr)	2014-09-26	2015-09-25	Compositions antitranspirantes et desodorisantes comprenant des compositions de reduction des mauvaises odeurs
CA2959691A Abandoned CA2959691A1 (fr)	2014-09-26	2015-09-25	Produits comprenant des matieres de reduction des mauvaises odeurs

Family Applications Before (6)

Application Number	Title	Priority Date	Filing Date
CA2959432A Abandoned CA2959432A1 (fr)	2014-09-26	2015-09-25	Compositions de reduction des mauvaises odeurs
CA2960394A Pending CA2960394A1 (fr)	2014-09-26	2015-09-25	Compositions rafraichissantes et dispositifs comprenant celles-ci
CA2959697A Pending CA2959697A1 (fr)	2014-09-26	2015-09-25	Systemes d'administration comprenant des compositions de reduction des mauvaises odeurs
CA2960390A Pending CA2960390A1 (fr)	2014-09-26	2015-09-25	Compositions rafraichissantes et dispositifs les comprenant
CA2959546A Abandoned CA2959546A1 (fr)	2014-09-26	2015-09-25	Compositions de nettoyage et/ou de traitement comportant des compositions de reduction de mauvaises odeurs
CA2959555A Pending CA2959555A1 (fr)	2014-09-26	2015-09-25	Procede de fabrication d'articles parfumes

Family Applications After (2)

Application Number	Title	Priority Date	Filing Date
CA2959434A Active CA2959434C (fr)	2014-09-26	2015-09-25	Compositions antitranspirantes et desodorisantes comprenant des compositions de reduction des mauvaises odeurs
CA2959691A Abandoned CA2959691A1 (fr)	2014-09-26	2015-09-25	Produits comprenant des matieres de reduction des mauvaises odeurs

Country Status (10)

Country	Link
US (20)	US10113140B2 (fr)
EP (10)	EP3197425A1 (fr)
JP (10)	JP2017530122A (fr)
KR (2)	KR101971378B1 (fr)
CN (8)	CN106687099A (fr)
AR (1)	AR105148A1 (fr)
CA (9)	CA2959432A1 (fr)
MX (7)	MX2017003966A (fr)
WO (11)	WO2016049398A1 (fr)
ZA (1)	ZA201701449B (fr)

Families Citing this family (139)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US11085009B2 (en) *	2012-10-12	2021-08-10	International Flavors & Fragrances Inc.	Enhanced deposition of ethyl vanillin or vanillin with friable microcapsules
MX352379B (es)	2013-04-05	2017-11-17	Procter & Gamble	Composicion para el cuidado personal que comprende una formulacion preemulsionada.
MX2017003966A (es)	2014-09-26	2017-06-30	Procter & Gamble	Composiciones de tratamiento y/o limpieza que comprenden composiciones para reducir el mal olor.
US10806688B2 (en)	2014-10-03	2020-10-20	The Procter And Gamble Company	Method of achieving improved volume and combability using an anti-dandruff personal care composition comprising a pre-emulsified formulation
US9993404B2 (en)	2015-01-15	2018-06-12	The Procter & Gamble Company	Translucent hair conditioning composition
WO2016117523A1 (fr) *	2015-01-19	2016-07-28	花王株式会社	Matériau pour article absorbant, procédé de fabrication de celui-ci, et article absorbant utilisant celui-ci
EP3262233A1 (fr)	2015-02-25	2018-01-03	The Procter and Gamble Company	Structures fibreuses comprenant une composition de ramollissement en surface
JP6663174B2 (ja) *	2015-06-08	2020-03-11	大日本除蟲菊株式会社	薬剤組成物、害虫防除用線香、及び加熱蒸散用製剤
WO2017004338A1 (fr)	2015-06-30	2017-01-05	The Procter & Gamble Company	Compositions contenant de multiples populations de microcapsules
EP3316974A1 (fr) *	2015-06-30	2018-05-09	The Procter and Gamble Company	Procédés de fabrication de compositions contenant plusieurs populations de microcapsules
PL3316854T3 (pl)	2015-06-30	2020-04-30	The Procter & Gamble Company	Kompozycja zawierająca wiele populacji mikrokapsułek zawierających środek zapachowy
WO2017011253A1 (fr)	2015-07-10	2017-01-19	The Procter & Gamble Company	Structures fibreuses comprenant une composition de ramollissement de surface
EP4434963A3 (fr) *	2015-09-08	2024-12-18	Symrise AG	Mélanges de parfum
US9714401B2 (en) *	2015-10-19	2017-07-25	The Procter & Gamble Company	Particles for malodor reduction
GB201521861D0 (en) *	2015-12-11	2016-01-27	Givaudan Sa	Improvements in or relating to organic compounds
DE102015225694A1 (de) *	2015-12-17	2017-06-22	Henkel Ag & Co. Kgaa	Treibmittelhaltige Deodorant- und/oder Antitranspirantien mit speziellen Konservierungsmittelkombinationen
CN116831927A (zh)	2016-01-20	2023-10-03	宝洁公司	包含单烷基甘油基醚的毛发调理组合物
EP4471114A3 (fr) *	2016-02-24	2025-03-19	Takasago International Corporation	Bloc de rebord de toilettes ou bloc de réservoir de toilettes fournissant des sensations de refroidissement
EP4410937A2 (fr) *	2016-02-24	2024-08-07	Takasago International Corporation	Dispositif de distribution de désodorisant alimenté électriquement fournissant des sensations de réchauffement et/ou de picotement
CN108697599B (zh)	2016-03-24	2024-09-17	宝洁公司	包含恶臭减少组合物的毛发护理组合物
US10457900B2 (en) *	2016-05-20	2019-10-29	The Proctor & Gamble Company	Detergent composition comprising an alkyl ether sulfate-rich surfactant system and coated encapsulates
US10494592B2 (en) *	2016-05-20	2019-12-03	The Procter & Gamble Company	Detergent composition comprising anionic/nonionic/cationic surfactant system and encapsulates
US20170355933A1 (en) *	2016-06-09	2017-12-14	The Procter & Gamble Company	Cleaning compositions including nuclease enzyme and malodor reduction materials
FR3052665B1 (fr) *	2016-06-16	2018-06-08	Expressions Parfumees	Melange comprenant au moins de la dihydro-5-pentyl-2(3h)-furanone et du 2,4-dimethyl-4-phenyltetrahydrofurane et son utilisation pour masquer les mauvaises odeurs
GB2551395A (en)	2016-06-17	2017-12-20	Reckitt Benckiser (Brands) Ltd	Atomiser system for dispensing a fragrance
US11097031B2 (en)	2016-08-01	2021-08-24	The Procter & Gamble Company	Phase-stable, sprayable freshening compositions comprising suspended particles
US10076583B2 (en) *	2016-08-01	2018-09-18	The Procter & Gamble Company	Phase-stable, sprayable freshening compositions comprising suspended particles and methods of freshening the air or a surface with the same
CN114588299A (zh)	2016-08-01	2022-06-07	宝洁公司	包含悬浮颗粒的相稳定的可喷雾清新组合物
WO2018026625A1 (fr) *	2016-08-01	2018-02-08	The Procter & Gamble Company	Produit rafraîchissant pulvérisable comprenant des particules en suspension et procédés de rafraîchissement de l'air ou d'une surface à l'aide de celui-ci
EP3279303B2 (fr) *	2016-08-04	2022-03-23	The Procter & Gamble Company	Article de dose unitaire soluble dans l'eau comprenant un tensioactif amphotère
US10894932B2 (en)	2016-08-18	2021-01-19	The Procter & Gamble Company	Fabric care composition comprising glyceride copolymers
WO2018053344A1 (fr) *	2016-09-16	2018-03-22	University Of Florida Research Foundation, Inc.	Compositions volatiles renforçant la sucrosité et procédés d'augmentation de la sucrosité perçue d'un produit comestible
DE102016219295A1 (de) *	2016-09-26	2018-03-29	Henkel Ag & Co. Kgaa	Kontinuierliches Verfahren zur Herstellung parfümhaltiger Schmelzkörper
EP3301160A1 (fr) *	2016-10-03	2018-04-04	The Procter & Gamble Company	Composition de détergent pour lessive à bas ph
EP3535367B1 (fr)	2016-11-01	2024-08-07	The Procter & Gamble Company	Leuco-colorants utilisés en tant qu'agents d'azurage dans des compositions d'entretien du linge
BR112019006576A2 (pt)	2016-11-01	2019-07-02	Milliken & Co	corantes leuco como agentes de azulamento em composições de cuidados de lavanderia
CN109890949B (zh)	2016-11-01	2021-10-01	宝洁公司	衣物洗涤护理组合物中作为上蓝剂的隐色着色剂、其包装、试剂盒和方法
US10870816B2 (en)	2016-11-18	2020-12-22	The Procter & Gamble Company	Fabric treatment compositions having low calculated cationic charge density polymers and fabric softening actives and methods for providing a benefit
CN120242113A (zh) *	2016-11-18	2025-07-04	弗门尼舍有限公司	使用挥发性成分来限制或消除对粪便恶臭的感知
EP3541913A1 (fr)	2016-11-18	2019-09-25	The Procter and Gamble Company	Compositions de traitement de tissu et procédés apportant un bénéfice
US20180142188A1 (en) *	2016-11-18	2018-05-24	The Procter & Gamble Company	Fabric treatment compositions having polymers and fabric softening actives and methods for providing a benefit
WO2018094314A1 (fr)	2016-11-21	2018-05-24	Bell Flavors & Fragrances, Inc.	Composition de neutralisation des mauvaises odeurs et méthodes
GB201703706D0 (en) *	2017-03-08	2017-04-19	Givaudan Sa	Improvements in or relating to organic compounds
JP7091365B2 (ja)	2017-05-05	2022-06-27	シムライズアーゲー	臭気を改善するための組成物
JP6895804B2 (ja) *	2017-05-29	2021-06-30	花王株式会社	鋳型造型用硬化剤組成物
EP3649184A1 (fr)	2017-07-06	2020-05-13	The Procter and Gamble Company	Composés de silicone
US20190010427A1 (en)	2017-07-06	2019-01-10	The Procter & Gamble Company	Silicone compounds
US10179887B1 (en) *	2017-07-14	2019-01-15	International Flavors & Fragrances Inc.	Organoleptic compounds
US20190029928A1 (en) *	2017-07-31	2019-01-31	The Procter & Gamble Company	Fibrous Structures Comprising Malodor Reduction Compositions
CN111108090A (zh) *	2017-09-25	2020-05-05	高砂香料工业株式会社	香料前体
WO2019061375A1 (fr) *	2017-09-30	2019-04-04	The Procter & Gamble Company	Procédé et appareil de démonstration visuelle des atouts de lutte contre les mauvaises odeurs de produits de consommation
EP4108228A1 (fr)	2017-10-10	2022-12-28	The Procter & Gamble Company	Composition d'hygiène personnelle transparente sans sulfate comprenant un sel inorganique faible
TWI715878B (zh)	2017-10-12	2021-01-11	美商美力肯及公司	隱色著色劑及組成物
WO2019075148A1 (fr)	2017-10-12	2019-04-18	The Procter & Gamble Company	Leuco-colorants en tant qu'agents d'azurage dans des compositions d'entretien du linge
WO2019075144A1 (fr)	2017-10-12	2019-04-18	The Procter & Gamble Company	Colorants leuco en combinaison avec un second agent de blanchiment en tant qu'agents d'azurage dans des compositions de soin du linge
EP3694972A1 (fr)	2017-10-12	2020-08-19	The Procter and Gamble Company	Leuco-colorants en tant qu'agents d'azurage dans des compositions d'entretien du linge
EP3704193A1 (fr)	2017-11-01	2020-09-09	Milliken & Company	Leucodérivés, composés colorants, et compositions les contenant
WO2019101821A2 (fr) *	2017-11-22	2019-05-31	Firmenich Sa	Utilisation de compositions volatiles pour limiter ou éliminer la perception des mauvaises odeurs fécales
CN111295204A (zh)	2017-11-22	2020-06-16	弗门尼舍有限公司	作为恶臭抵消成分的螺化合物
JP7460981B2 (ja) *	2017-11-29	2024-04-03	山本香料株式会社	アスファルト、汚泥、汚水、銀杏、堆肥、海獣、野菜、生ゴミ又は塗料の臭いの変調用臭気変調剤、及びアスファルト、汚泥、汚水、銀杏、堆肥、海獣、野菜、生ゴミ又は塗料の臭いの臭気変調方法
KR101988012B1 (ko) *	2017-12-12	2019-06-11	한국콜마주식회사	화장료 원료취 차폐용 조성물
US10792384B2 (en) *	2017-12-15	2020-10-06	The Procter & Gamble Company	Rolled fibrous structures comprising encapsulated malodor reduction compositions
JP6973220B2 (ja) *	2018-03-20	2021-11-24	日油株式会社	アスファルト用消臭剤
WO2019194186A1 (fr) *	2018-04-02	2019-10-10	花王株式会社	Composition de type musc
GB201805435D0 (en) *	2018-04-03	2018-05-16	Givaudan Sa	Improvements in or relating to organic compounds
US10699960B2 (en)	2018-06-27	2020-06-30	Taiwan Semiconductor Manufacturing Co., Ltd.	Methods for improving interlayer dielectric layer topography
CA3102399C (fr) *	2018-06-29	2023-03-14	The Procter & Gamble Company	Compositions de nettoyage comprenant des esteramines
US11015144B2 (en)	2018-06-29	2021-05-25	Ecolab Usa Inc.	Formula design for a solid laundry fabric softener
JP2021530604A (ja) *	2018-07-19	2021-11-11	ロンザ，エルエルシー	洗剤組成物
US11806448B2 (en)	2018-07-31	2023-11-07	Arylessence, Inc.	Freshening compositions comprising controlled release modulators
EP3848444A1 (fr) *	2018-08-14	2021-07-14	The Procter & Gamble Company	Compositions liquides pour le traitement de tissus comprenant un agent de blanchiment
EP3611247B1 (fr)	2018-08-14	2021-03-10	The Procter & Gamble Company	Compositions de traitement de tissus comprenant des capsules d'agent traitant
EP3848442A1 (fr)	2018-08-14	2021-07-14	The Procter & Gamble Company	Compositions de traitement de tissus comprenant des capsules d'agent traitant
CN109135960B (zh) *	2018-09-29	2021-05-04	广州立白企业集团有限公司	一种聚合物在洗涤剂中作为蛋白酶稳定剂的用途及洗涤剂组合物
US11299591B2 (en)	2018-10-18	2022-04-12	Milliken & Company	Polyethyleneimine compounds containing N-halamine and derivatives thereof
US20200123319A1 (en) *	2018-10-18	2020-04-23	Milliken & Company	Polyethyleneimine compounds containing n-halamine and derivatives thereof
US11732218B2 (en)	2018-10-18	2023-08-22	Milliken & Company	Polyethyleneimine compounds containing N-halamine and derivatives thereof
US11518963B2 (en)	2018-10-18	2022-12-06	Milliken & Company	Polyethyleneimine compounds containing N-halamine and derivatives thereof
US11466122B2 (en)	2018-10-18	2022-10-11	Milliken & Company	Polyethyleneimine compounds containing N-halamine and derivatives thereof
US20200123475A1 (en) *	2018-10-18	2020-04-23	Milliken & Company	Polyethyleneimine compounds containing n-halamine and derivatives thereof
CN113056547A (zh) *	2018-11-19	2021-06-29	西姆莱斯有限公司	茉莉醇
US20200170906A1 (en) *	2018-12-04	2020-06-04	The Procter & Gamble Company	Hair care composition for cleansing and refreshing the hair and the scalp
ES2984058T3 (es)	2019-01-17	2024-10-28	Firmenich & Cie	Composición antitranspirante o desodorante
AU2020272127B2 (en)	2019-04-12	2022-12-08	Ecolab Usa Inc.	Antimicrobial multi-purpose cleaner and methods of making and using the same
JP7385999B2 (ja) *	2019-05-24	2023-11-24	株式会社資生堂	パーソナルケア組成物および悪臭抑制方法
JP7630441B2 (ja)	2019-05-31	2025-02-17	フイルメニツヒソシエテアノニム	節足動物防除組成物
CN114727602A (zh) *	2019-10-10	2022-07-08	宝洁公司	空气清新产品
KR102130972B1 (ko) *	2019-10-22	2020-07-07	한국화학연구원	탈취제용 조성물 및 이를 포함하는 탈취제
EP3822334A1 (fr) *	2019-11-18	2021-05-19	The Procter & Gamble Company	Procédé de réduction de mauvaises odeurs sur des tissus
EP3934703A1 (fr) *	2019-12-04	2022-01-12	Firmenich SA	Procédé et substrat à émanation pour la diffusion de parfum
BR112022010474A2 (pt)	2019-12-06	2022-09-06	Procter & Gamble	Composição isenta de sulfato com deposição acentuada de ativo sobre o couro cabeludo
CN110917867A (zh) *	2019-12-20	2020-03-27	烟台欧顺生物科技有限公司	一种微生物胞外多糖复合海藻多糖的异味去除剂的制备方法
TWI726626B (zh) *	2020-02-19	2021-05-01	大陸商廣州市創韋照明燈具有限公司	適合產生煙霧的含醣類水溶液配方及使用含醣類水溶液產生煙霧的方法
EP4110474A1 (fr)	2020-02-27	2023-01-04	The Procter & Gamble Company	Compositions antipelliculaires contenant du soufre ayant une efficacité et une esthétique améliorées
CN115151340A (zh) *	2020-02-28	2022-10-04	杰富意矿物股份有限公司	复合体
US20230151161A1 (en)	2020-04-09	2023-05-18	Tyromer Inc.	Method and system for odour abatement in rubber processing
WO2021228352A1 (fr) *	2020-05-11	2021-11-18	Symrise Ag	Composition de parfum
US11807829B2 (en)	2020-06-05	2023-11-07	The Procter & Gamble Company	Detergent compositions containing a branched surfactant
US20220056371A1 (en) *	2020-08-18	2022-02-24	Ap Goldshield Llc	3-in one fabric conditioners and softeners comprising antimicrobial agents
MX2023003016A (es)	2020-09-22	2023-04-10	Swimc Llc	Composiciones de recubrimiento que contienen quitosana.
US20230363992A1 (en) *	2020-09-28	2023-11-16	Kdc/One Development Corporation, Inc.	Silicone-free antiperspirant and deodorant compositions
EP4237498A1 (fr)	2020-10-27	2023-09-06	Milliken & Company	Compositions comprenant des composés leuco et des colorants
CN112611823A (zh) *	2020-11-18	2021-04-06	上海和黄药业有限公司	一种药物制剂中冰片和人工麝香的主要活性成分的检测方法
CN116568263A (zh) *	2020-12-04	2023-08-08	宝洁公司	包含恶臭减少材料的毛发护理组合物
KR20230119174A (ko) *	2020-12-09	2023-08-16	시므라이즈 아게	1,2-알칸디올들을 포함하는 혼합물
US11560534B2 (en)	2020-12-15	2023-01-24	Henkel Ag & Co. Kgaa	Surfactant compositions for improved transparency of DADMAC-acrylamide co-polymers
US11505766B2 (en)	2020-12-15	2022-11-22	Henkel Ag & Co. Kgaa	Surfactant compositions for improved transparency of DADMAC-acrylic acid co-polymers
KR102579965B1 (ko) *	2021-02-03	2023-09-19	한국콜마주식회사	어진향차 향취 재현 향료 조성물
EP4050089A1 (fr) *	2021-02-25	2022-08-31	The Procter & Gamble Company	Procédé de traitement d'un tissu dans un séchoir en présence de micro-organismes
US20220378684A1 (en)	2021-05-14	2022-12-01	The Procter & Gamble Company	Shampoo Compositions Containing a Sulfate-Free Surfactant System and Sclerotium Gum Thickener
WO2022251818A1 (fr)	2021-05-26	2022-12-01	The Procter & Gamble Company	Composés d'agent pro-bénéfice avec des fractions hétérocycliques
US11986543B2 (en)	2021-06-01	2024-05-21	The Procter & Gamble Company	Rinse-off compositions with a surfactant system that is substantially free of sulfate-based surfactants
EP4319716A1 (fr) *	2021-06-03	2024-02-14	Firmenich SA	Compositions pour limiter, réduire ou éliminer les mauvaises odeurs associées à des matières plastiques
EP4376793A1 (fr) *	2021-07-28	2024-06-05	Shear/Kershman Laboratories, Inc.	Lotion antiseptique contenant du formaldéhyde à odeur réduite
WO2023019221A1 (fr) *	2021-08-13	2023-02-16	Encapsys, Llc	Articles de fabrication avec des particules de diffusion dégradables à base de matières naturelles contenant une amine
CN113841707B (zh) *	2021-10-26	2022-07-05	中国热带农业科学院环境与植物保护研究所	反式法尼醇作为增效剂在防治荔枝霜疫病中的应用
GB202204394D0 (en) *	2022-03-28	2022-05-11	Codikoat Ltd	Antimicrobial and/or antiviral materials
EP4321604A1 (fr)	2022-08-08	2024-02-14	The Procter & Gamble Company	Tissu et composition de soins à domicile comprenant un tensioactif et un polyester
EP4535997A1 (fr) *	2022-10-05	2025-04-16	Klura Ltd	Matériaux antimicrobiens et/ou antiviraux
WO2024094800A1 (fr)	2022-11-04	2024-05-10	The Procter & Gamble Company	Composition d'entretien textile et ménager
WO2024094778A1 (fr)	2022-11-04	2024-05-10	Clariant International Ltd	Polyesters
WO2024094803A1 (fr)	2022-11-04	2024-05-10	The Procter & Gamble Company	Composition d'entretien textile et ménager
WO2024119298A1 (fr)	2022-12-05	2024-06-13	The Procter & Gamble Company	Composition de soin textile et ménager comprenant un composé de carbonate de polyalkylène
WO2024129520A1 (fr)	2022-12-12	2024-06-20	The Procter & Gamble Company	Composition de soin textile et ménager
EP4386074A1 (fr)	2022-12-16	2024-06-19	The Procter & Gamble Company	Composition de soin pour le linge et le domicile
EP4411059A3 (fr)	2023-02-06	2024-08-21	Kraton Polymers Nederland B.V.	Compositions et procédés de lutte contre les odeurs
GB202303310D0 (en)	2023-03-07	2023-04-19	Joulium Energy Ltd	Working fluid composition
WO2024213536A1 (fr) *	2023-04-13	2024-10-17	Givaudan Sa	Composition de parfum
EP4458932A1 (fr)	2023-05-04	2024-11-06	The Procter & Gamble Company	Tissu et composition de soins à domicile
EP4458933A1 (fr)	2023-05-05	2024-11-06	The Procter & Gamble Company	Composition de tissu et de soins à domicile comprenant un polyol propoxylé
EP4484536A1 (fr)	2023-06-26	2025-01-01	The Procter & Gamble Company	Composition de soin pour le linge et le domicile
US20250034489A1 (en) *	2023-07-28	2025-01-30	The Procter & Gamble Company	Dryer sheet and process of making
WO2025053198A1 (fr) *	2023-09-07	2025-03-13	高砂香料工業株式会社	Composition d'odeur semi-sèche et composition de parfum de masquage
EP4549540A1 (fr)	2023-11-02	2025-05-07	The Procter & Gamble Company	Composition de soin pour le linge et le domicile
EP4549541A1 (fr)	2023-11-02	2025-05-07	The Procter & Gamble Company	Composition de soin pour le linge et le domicile
EP4553137A1 (fr)	2023-11-08	2025-05-14	The Procter & Gamble Company	Composition de soin domestique et de tissu comprenant un polyester
EP4570893A1 (fr)	2023-12-15	2025-06-18	The Procter & Gamble Company	Composition de soin pour le linge et le domicile
EP4570892A1 (fr)	2023-12-15	2025-06-18	The Procter & Gamble Company	Composition de détergent à lessive
KR102789509B1 (ko) *	2024-06-26	2025-03-31	백남현	방향제 및 이의 제조방법

Family Cites Families (173)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2438091A (en)	1943-09-06	1948-03-16	American Cyanamid Co	Aspartic acid esters and their preparation
US2528378A (en)	1947-09-20	1950-10-31	John J Mccabe Jr	Metal salts of substituted quaternary hydroxy cycloimidinic acid metal alcoholates and process for preparation of same
US2658072A (en)	1951-05-17	1953-11-03	Monsanto Chemicals	Process of preparing amine sulfonates and products obtained thereof
US2809971A (en)	1955-11-22	1957-10-15	Olin Mathieson	Heavy-metal derivatives of 1-hydroxy-2-pyridinethiones and method of preparing same
US3236733A (en)	1963-09-05	1966-02-22	Vanderbilt Co R T	Method of combatting dandruff with pyridinethiones metal salts detergent compositions
US3761418A (en)	1967-09-27	1973-09-25	Procter & Gamble	Detergent compositions containing particle deposition enhancing agents
US3904741A (en)	1970-10-26	1975-09-09	Armour Pharma	Alcohol soluble basic aluminum chlorides and method of making same
CA958338A (en)	1971-03-08	1974-11-26	Chung T. Shin	Antiperspirant powder aerosol compositions containing aluminum chloride and water soluble aluminum compounds and methods of preparation
US3792068A (en)	1971-04-02	1974-02-12	Procter & Gamble	Dry powder aerosol antiperspirant composition incorporating dry powder antiperspirant active complex and process for its preparation
US3716498A (en)	1971-04-02	1973-02-13	Int Flavors & Fragrances Inc	Novel fragrance compositions
US3753196A (en)	1971-10-05	1973-08-14	Kulite Semiconductor Products	Transducers employing integral protective coatings and supports
US3887692A (en)	1972-07-10	1975-06-03	Armour Pharma	Microspherical basic aluminum halides and method of making same
US4049792A (en)	1973-06-26	1977-09-20	The Procter & Gamble Company	Antiperspirant stick
DE2504381A1 (de)	1974-02-04	1975-12-18	Procter & Gamble	Zirkonium- und hafniumsalze und ihre komplexe mit aluminiumverbindungen und aminosaeuren, verfahren zur herstellung dieser salze und komplexe sowie antiperspirationsmittel, die diese komplexe enthalten
US4359456A (en)	1976-01-14	1982-11-16	Lever Brothers Company	Antiperspirant activity of basic aluminum compounds
GB1567947A (en)	1976-07-02	1980-05-21	Unilever Ltd	Esters of quaternised amino-alcohols for treating fabrics
US4120948A (en)	1976-11-29	1978-10-17	The Procter & Gamble Company	Two phase antiperspirant compositions
US4237155A (en)	1979-04-30	1980-12-02	The Procter & Gamble Company	Articles and methods for treating fabrics
GB2048229A (en)	1979-04-20	1980-12-10	Gillette Co	Aluminium Chlorhydroxide and Preparation Thereof
EP0028853B2 (fr)	1979-11-07	1988-11-02	THE PROCTER & GAMBLE COMPANY	Compositions antiperspirantes
US4379753A (en)	1980-02-07	1983-04-12	The Procter & Gamble Company	Hair care compositions
US4323683A (en)	1980-02-07	1982-04-06	The Procter & Gamble Company	Process for making pyridinethione salts
US4345080A (en)	1980-02-07	1982-08-17	The Procter & Gamble Company	Pyridinethione salts and hair care compositions
US4470982A (en)	1980-12-22	1984-09-11	The Procter & Gamble Company	Shampoo compositions
GR76237B (fr)	1981-08-08	1984-08-04	Procter & Gamble
JPS604598A (ja) *	1983-06-22	1985-01-11	ライオン株式会社	防臭性洗浄剤組成物
GB2144992A (en)	1983-08-16	1985-03-20	Gillette Co	Antiperspirants
JPS62205200A (ja) *	1986-03-03	1987-09-09	花王株式会社	芳香性液体漂白剤組成物
US5942217A (en)	1997-06-09	1999-08-24	The Procter & Gamble Company	Uncomplexed cyclodextrin compositions for odor control
US4973416A (en) *	1988-10-14	1990-11-27	The Procter & Gamble Company	Liquid laundry detergent in water-soluble package
US4985238A (en)	1989-03-14	1991-01-15	The Procter & Gamble Company	Low residue antiperspirant sticks
US5019375A (en)	1989-03-14	1991-05-28	The Procter & Gamble Company	Low residue antiperspirant creams
US5104646A (en)	1989-08-07	1992-04-14	The Procter & Gamble Company	Vehicle systems for use in cosmetic compositions
US5106609A (en)	1990-05-01	1992-04-21	The Procter & Gamble Company	Vehicle systems for use in cosmetic compositions
DE4015849A1 (de)	1990-05-17	1991-11-21	Henkel Kgaa	Quaternierte ester
ES2104850T3 (es) *	1991-11-08	1997-10-16	Quest Int	Composicion de perfume.
WO1993023008A1 (fr)	1992-05-12	1993-11-25	The Procter & Gamble Company	Composition de gel antisudoral en baton
EP0571677A1 (fr)	1992-05-29	1993-12-01	Unilever Plc	Microémulsions aqueuses de parfums
JPH06220495A (ja) *	1993-01-25	1994-08-09	Lion Corp	液体漂白剤組成物
US5486303A (en)	1993-08-27	1996-01-23	The Procter & Gamble Company	Process for making high density detergent agglomerates using an anhydrous powder additive
US5714137A (en)	1994-08-12	1998-02-03	The Procter & Gamble Company	Uncomplexed cyclodextrin solutions for odor control on inanimate surfaces
US5670475A (en)	1994-08-12	1997-09-23	The Procter & Gamble Company	Composition for reducing malodor impression of inanimate surfaces
JP3810433B2 (ja) *	1994-08-12	2006-08-16	ザプロクターアンドギャンブルカンパニー	非生物表面で悪臭印象を減少させるための組成物
HU218030B (hu) *	1994-08-12	2000-05-28	The Procter & Gamble Co.	Nem komplexált ciklodextrin-oldatok élettelen felületek szagtalanítására és alkalmazásuk
US5879584A (en)	1994-09-10	1999-03-09	The Procter & Gamble Company	Process for manufacturing aqueous compositions comprising peracids
US5516448A (en)	1994-09-20	1996-05-14	The Procter & Gamble Company	Process for making a high density detergent composition which includes selected recycle streams for improved agglomerate
US5691297A (en)	1994-09-20	1997-11-25	The Procter & Gamble Company	Process for making a high density detergent composition by controlling agglomeration within a dispersion index
US5489392A (en)	1994-09-20	1996-02-06	The Procter & Gamble Company	Process for making a high density detergent composition in a single mixer/densifier with selected recycle streams for improved agglomerate properties
US5534179A (en)	1995-02-03	1996-07-09	Procter & Gamble	Detergent compositions comprising multiperacid-forming bleach activators
US5574005A (en)	1995-03-07	1996-11-12	The Procter & Gamble Company	Process for producing detergent agglomerates from high active surfactant pastes having non-linear viscoelastic properties
US5569645A (en)	1995-04-24	1996-10-29	The Procter & Gamble Company	Low dosage detergent composition containing optimum proportions of agglomerates and spray dried granules for improved flow properties
US5597936A (en)	1995-06-16	1997-01-28	The Procter & Gamble Company	Method for manufacturing cobalt catalysts
US5565422A (en)	1995-06-23	1996-10-15	The Procter & Gamble Company	Process for preparing a free-flowing particulate detergent composition having improved solubility
US5576282A (en)	1995-09-11	1996-11-19	The Procter & Gamble Company	Color-safe bleach boosters, compositions and laundry methods employing same
US5800897A (en)	1996-01-25	1998-09-01	Eastman Chemical Company	Air freshener composition containing a fiber pad
JPH1017894A (ja) *	1996-07-04	1998-01-20	Kao Corp	液体漂白剤組成物
US5891425A (en)	1996-10-29	1999-04-06	Procter & Gamble Company	Antiperspirant cream composition having improved rheology
US6225464B1 (en)	1997-03-07	2001-05-01	The Procter & Gamble Company	Methods of making cross-bridged macropolycycles
US6656923B1 (en)	1997-06-09	2003-12-02	The Procter & Gamble Company	Uncomplexed cyclodextrin compositions for odor and wrinkle control
US6180121B1 (en)	1998-03-05	2001-01-30	Colgate-Palmolive Company	Fragrance enhancing compositions for cosmetic products
GB9809772D0 (en)	1998-05-07	1998-07-08	Quest Int	Perfume composition
ATE367845T1 (de)	1998-06-15	2007-08-15	Procter & Gamble	Riechstoffzusammensetzungen
US6413920B1 (en)	1998-07-10	2002-07-02	Procter & Gamble Company	Amine reaction compounds comprising one or more active ingredient
GB9821693D0 (en)	1998-10-06	1998-12-02	Humphries Martyn	Improvements in or relating to insect repellents
US5976514A (en)	1998-11-20	1999-11-02	Procter & Gamble Company	Low-irritation antiperspirant and deodorant compositions containing a volatile, nonpolar hydrocarbon liquid
EP1133322B1 (fr)	1998-11-25	2003-09-24	The Procter & Gamble Company	Compositions ameliorees de cyclodextrine non mises en complexe servant a lutter contre les odeurs
AU2026100A (en)	1998-11-30	2000-06-19	Procter & Gamble Company, The	Process for preparing cross-bridged tetraaza macrocycles
JP2000178586A (ja) *	1998-12-17	2000-06-27	Lion Corp	自動食器洗浄機用洗浄剤組成物
US6488943B1 (en)	1999-04-13	2002-12-03	The Procter & Gamble Company	Antimicrobial wipes which provide improved immediate germ reduction
JP2001011497A (ja) *	1999-06-30	2001-01-16	Lion Corp	薄肉プラスチックボトルに充填された液体洗浄剤製品
JP3617613B2 (ja) *	1999-06-30	2005-02-09	ライオン株式会社	液体洗浄剤組成物
EP1067173A1 (fr) *	1999-07-08	2001-01-10	The Procter & Gamble Company	Procédé de production de particules de produit de réaction d'amine
EP1067174B1 (fr) *	1999-07-08	2004-09-29	The Procter & Gamble Company	Procédé de production de particules de produit de réaction d'amine
US6386392B1 (en)	1999-11-02	2002-05-14	The Procter & Gamble Company	Reservoirs for use with cleaning devices
US6716805B1 (en)	1999-09-27	2004-04-06	The Procter & Gamble Company	Hard surface cleaning compositions, premoistened wipes, methods of use, and articles comprising said compositions or wipes and instructions for use resulting in easier cleaning and maintenance, improved surface appearance and/or hygiene under stress conditions such as no-rinse
US6814088B2 (en)	1999-09-27	2004-11-09	The Procter & Gamble Company	Aqueous compositions for treating a surface
JP2003501558A (ja) *	1999-11-18	2003-01-14	ザ、プロクター、エンド、ギャンブル、カンパニー	臭いを制御するための改良された非錯化シクロデキストリン組成物
JP3566171B2 (ja) *	2000-03-09	2004-09-15	花王株式会社	液体洗浄剤組成物
ATE332955T1 (de) *	2000-05-24	2006-08-15	Procter & Gamble	Gewebeweichmacherzusammensetzung mit geruchskontrollmittel
US20040028551A1 (en)	2000-07-27	2004-02-12	Kvietok Frank Andrej	Methods for emitting volatile compositions
US6610648B2 (en) *	2000-12-22	2003-08-26	Givaudan Sa	Malodor counteractant compositions
ES2247316T3 (es) *	2001-02-14	2006-03-01	THE PROCTER & GAMBLE COMPANY	Composiciones para lavavajillas que comprenden un agente blanqueador de tipo peroxido de diacilo y un perfume floral.
JP2002336337A (ja) *	2001-05-14	2002-11-26	Lion Corp	消臭防汚剤
DE10132003A1 (de)	2001-07-03	2003-01-30	Merz & Co Gmbh & Co	Fett(öl)haltiges Mittel, enthaltend Zwiebelextrakt, seine Herstellung und seine Verwendung zur Pflege, Vorbeugung oder Behandlung von geschädigtem Hautgewebe, insbesondere von Narben
JP2003082398A (ja) *	2001-09-11	2003-03-19	Lion Corp	洗浄剤製品
JP2003171688A (ja) *	2001-12-05	2003-06-20	Lion Corp	中性液体洗浄剤組成物
JP2003176497A (ja) *	2001-12-10	2003-06-24	Lion Corp	ガラス用洗浄剤組成物
JP2003268398A (ja) *	2002-03-15	2003-09-25	Lion Corp	液体漂白性組成物
US6722529B2 (en)	2002-04-15	2004-04-20	Michael J. Ceppaluni	Air flow scent enhancer
WO2003089312A2 (fr)	2002-04-17	2003-10-30	Playtex Products, Inc.	Cassette jetable destinee a une extraction sequentielle d'un plastique tubulaire a capacite de neutralisation des mauvaises odeurs
JP4579509B2 (ja) *	2002-08-09	2010-11-10	花王株式会社	香料組成物
US7172099B2 (en)	2002-09-09	2007-02-06	The Procter & Gamble Company	Fluid delivery mechanism
US9035123B2 (en)	2002-10-01	2015-05-19	The Procter & Gamble Company	Absorbent article having a lotioned topsheet
US8187580B2 (en) *	2002-11-01	2012-05-29	The Procter & Gamble Company	Polymeric assisted delivery using separate addition
WO2006043177A1 (fr)	2004-10-20	2006-04-27	Firmenich Sa	Systemes de solubilisation d'aromes et de parfums
US7202198B2 (en)	2003-06-10	2007-04-10	International Flavors & Fragrances Inc.	Substituted phenolic composition and process for using same for inhibiting malodours
US20050003975A1 (en) *	2003-06-18	2005-01-06	Browne Yvonne Bridget	Blooming soap bars
US7365043B2 (en)	2003-06-27	2008-04-29	The Procter & Gamble Co.	Lipophilic fluid cleaning compositions capable of delivering scent
DE10330865A1 (de)	2003-07-09	2005-01-27	Symrise Gmbh & Co. Kg	4,8-Dimethyl-7-nonen-2-on und 4,8-Dimethylnonan-2-on als Riechstoffe
AR045608A1 (es) *	2003-09-08	2005-11-02	Colgate Palmolive Co	Gel transparente antitranspirante con bajo contenido de glicol
US20080032245A1 (en) *	2003-11-11	2008-02-07	Vapor Fuel Technologies, Llc	Fuel utilization
CA2548454C (fr)	2003-12-04	2013-12-31	Kyowa Hakko Kogyo Co., Ltd.	Medicament comportant un anticorps recombinant contre le recepteur r4 de chimiokine cc
US20050192206A1 (en)	2004-02-27	2005-09-01	O'brien Janese C.	Methods and instructions for installing and removing a fabric conditioning article in a dryer
DE102004023720A1 (de) *	2004-05-11	2005-12-08	Henkel Kgaa	Verwendung von Cyclodextrin-Verbindungen als geruchsbindendes Mittel
US20050276831A1 (en)	2004-06-10	2005-12-15	Dihora Jiten O	Benefit agent containing delivery particle
JP4129645B2 (ja) *	2004-08-30	2008-08-06	ライオン株式会社	シャンプー組成物
JP4694171B2 (ja) *	2004-10-07	2011-06-08	ライオン株式会社	ノンエアゾール型泡吐出容器用ヘアリンス組成物およびノンエアゾール型泡吐出ヘアリンス製品
US8058500B2 (en) *	2005-05-06	2011-11-15	Kimberly-Clark Worldwide, Inc.	Malodor reduction patch
US20070003499A1 (en)	2005-06-30	2007-01-04	The Gillette Company	Particulate enhanced efficacy antiperspirant salt with raised pH
JP5038656B2 (ja) *	2005-11-18	2012-10-03	花王株式会社	消臭剤組成物
JP5138169B2 (ja) *	2005-12-27	2013-02-06	ライオン株式会社	液体漂白剤組成物
EP1989283A2 (fr) *	2006-02-28	2008-11-12	The Procter and Gamble Company	Particule pour libération contenant un agent avantageux
JP4243867B2 (ja) *	2006-03-29	2009-03-25	ライオン株式会社	ロスマリン酸含有組成物
WO2007127042A2 (fr) *	2006-04-26	2007-11-08	Johnson James H	Distributeur de materiau en bobine
CN101501174B (zh) *	2006-05-23	2013-08-21	宝洁公司	用于消费品的香料递送体系
US20070275866A1 (en) *	2006-05-23	2007-11-29	Robert Richard Dykstra	Perfume delivery systems for consumer goods
US20080003245A1 (en) *	2006-06-30	2008-01-03	Beiersdorf Ag	Use of octyl salicylate in cosmetic preparations containing 1,3-dihydroxyacetone
ES2530689T3 (es)	2006-09-04	2015-03-04	Takasago Perfumery Co Ltd	Encapsulación de moléculas de fragancia voluminosas
DE102006056320A1 (de) *	2006-11-21	2008-05-29	Beiersdorf Ag	Kosmetische Formulierung mit Glucosylglyceriden und ausgewählten Parfümstoffen
ATE460686T1 (de)	2006-12-20	2010-03-15	Agfa Graphics Nv	Flexodruckformvorläufer für lasergravur
WO2008090518A1 (fr)	2007-01-26	2008-07-31	Koninklijke Philips Electronics N.V.	Filtre de compensation de l'effet talon qui conserve le spectre, réalisé dans le même matériau qu'une plaque anodique
MX2009008576A (es)	2007-02-09	2009-08-18	Procter & Gamble	Sistemas de perfume.
DE102007019369A1 (de)	2007-04-23	2008-10-30	Henkel Ag & Co. Kgaa	Photokatalytisches Material enthaltende Partikel
DE102007028024A1 (de)	2007-06-14	2008-12-18	Beiersdorf Ag	Kosmetische oder dermatologische Zubereitungen mit einem Gehalt an molekularem Sauerstoff und Parfümstoffen
WO2008155683A1 (fr)	2007-06-18	2008-12-24	Firmenich Sa	Compositions agissant contre les mauvaises odeurs et leur procédé d'utilisation
CN101101299A (zh) *	2007-06-25	2008-01-09	华东理工大学	一种并-串联模式识别方法及其在机器嗅觉中的应用
US7550416B2 (en) *	2007-06-27	2009-06-23	The Procter & Gamble Company	Perfumed household products and methods for preserving perfume integrity and extending fragrance life
GB2450727A (en)	2007-07-05	2009-01-07	Irish Skincare Ltd	Perfumed silicone microemulsion
GB0718532D0 (en)	2007-09-22	2007-10-31	Unilever Plc	Improvements relating to fabric treatment compositions
CN102123742A (zh)	2008-02-22	2011-07-13	宝洁公司	包括含有凉爽剂的洗剂组合物的吸收制品
US20090312223A1 (en)	2008-06-13	2009-12-17	Conopco, Inc., D/B/A Unilever	Method of Controlling Structure and Rheology of Low Active Liquid Cleansers by Selecting Perfume Components
KR100905419B1 (ko) *	2008-09-11	2009-07-02	연세대학교 산학협력단	세스퀴테르펜 유도체의 용도
US20100190673A1 (en) *	2009-01-29	2010-07-29	Johan Smets	Encapsulates
DE102009001570A1 (de)	2009-03-16	2010-09-23	Henkel Ag & Co. Kgaa	Lilial-Surrogat
US8931711B2 (en)	2009-04-16	2015-01-13	The Procter & Gamble Company	Apparatus for delivering a volatile material
US8709337B2 (en)	2009-04-16	2014-04-29	The Procter & Gamble Company	Method for delivering a volatile material
MX2011012192A (es) *	2009-05-15	2011-12-08	Procter & Gamble	Sistema de perfume.
MX2011013546A (es)	2009-06-18	2012-01-20	Procter & Gamble	Composicion para el cuidado personal que comprende un polimero cationico sinteco.
CN102473248A (zh) *	2009-07-07	2012-05-23	宝洁公司	特性-空间相似度建模
CN102686721B (zh) *	2009-11-12	2016-02-10	Q医疗公司	用于哺乳动物来源的神经胶质限制性祖细胞的扩增、鉴定、表征和效能增强的方法和组合物
EP2512527A1 (fr) *	2009-12-17	2012-10-24	The Procter & Gamble Company	Compositions rafraîchissantes comprenant des polymères se liant aux mauvaises odeurs et des composants de suppression des mauvaises odeurs
EP3309245A1 (fr) *	2009-12-18	2018-04-18	The Procter & Gamble Company	Produits encapsulés
PL2555742T3 (pl) *	2010-04-06	2016-10-31		Enkapsulaty
JP2012526188A (ja) *	2010-04-06	2012-10-25	ザプロクターアンドギャンブルカンパニー	カプセル
US20110269657A1 (en)	2010-04-28	2011-11-03	Jiten Odhavji Dihora	Delivery particles
US9186642B2 (en) *	2010-04-28	2015-11-17	The Procter & Gamble Company	Delivery particle
US8322631B2 (en)	2010-05-10	2012-12-04	The Procter & Gamble Company	Trigger pump sprayer having favorable particle size distribution with specified liquids
JP5419799B2 (ja) *	2010-05-21	2014-02-19	花王株式会社	床用液体洗浄剤組成物
US8741275B2 (en)	2010-06-04	2014-06-03	Robetet, Inc.	Malodor neutralizing compositions comprising undecylenic acid or citric acid
CN102933190A (zh)	2010-06-11	2013-02-13	宝洁公司	用于处理皮肤的组合物
US9174229B2 (en)	2010-06-11	2015-11-03	The Procter & Gamble Company	Dispenser having non-frustro-conical funnel wall
WO2011163337A1 (fr)	2010-06-22	2011-12-29	The Procter & Gamble Company	Systèmes de parfum
JP5692844B2 (ja)	2010-09-24	2015-04-01	高砂香料工業株式会社	スルフィド類用消臭剤組成物
JP5711385B2 (ja) *	2010-12-08	2015-04-30	ザプロクターアンドギャンブルカンパニー	非芳香及び低芳香性悪臭抑制組成物並びにその方法
ES2819073T3 (es) *	2011-01-27	2021-04-14	Robertet Inc	Composiciones neutralizantes del mal olor que comprenden acetato de bornilo o acetato de isobornilo
US20120219610A1 (en)	2011-02-28	2012-08-30	Smith Iii Edward Dewey	Bar Compositions Comprising Platelet Zinc Pyrithione
US20120230936A1 (en) *	2011-03-09	2012-09-13	The Dial Corporation	Gel air freshener with improved length-of-life and method for producing same
JP2014513076A (ja)	2011-04-04	2014-05-29	ザプロクターアンドギャンブルカンパニー	パーソナルケア物品
DE102011006982A1 (de) *	2011-04-07	2012-10-11	Beiersdorf Ag	Zubereitungen mit einem langanhaltenden floralen Duft ohne 4-(4-Hydroxy-4-methylpentyl)-3-cyclohexencarboxaldehyd
US20120258150A1 (en) *	2011-04-11	2012-10-11	Holly Balasubramanian Rauckhorst	Particles comprising volatile materials and particle gas saturated solution processes for making same
US9296550B2 (en)	2013-10-23	2016-03-29	The Procter & Gamble Company	Recyclable plastic aerosol dispenser
WO2012162331A2 (fr) *	2011-05-26	2012-11-29	The Procter & Gamble Company	Compositions comprenant un bouquet efficace de parfums
WO2013018805A1 (fr) *	2011-08-01	2013-02-07	山本香料株式会社	Fragrance destinée à supprimer les odeurs fécales, fragrance encapsulée dans des microcapsules utilisant celle-ci, textile pouvant supprimer les odeurs fécales, pastilles destinées à supprimer les odeurs fécales, pulvérisation d'une fragrance encapsulée dans des microcapsules, et dispositif de pulvérisation d'un parfum destiné à supprimer les odeurs fécales
PH12014500361A1 (en)	2011-08-15	2021-07-12	Procter & Gamble	Conformable personal care articles
MX2014011397A (es) *	2012-04-10	2014-11-25	Procter & Gamble	Composiciones para reducir el mal olor.
US9320407B2 (en)	2012-06-04	2016-04-26	The Procter & Gamble Company	Floor cleaning appliance having disposable floor sheets and method of cleaning a floor therewith
CN102901779B (zh) *	2012-09-13	2014-07-23	中国烟草总公司郑州烟草研究院	一种基于香味成分的烟叶焦甜感口感特征的判别方法
JP6247540B2 (ja) *	2013-01-11	2017-12-13	大日本除蟲菊株式会社	蚊取線香
ES2662421T3 (es)	2013-01-22	2018-04-06	The Procter & Gamble Company	Composiciones tratantes que comprenden microcápsulas, aminas primarias o secundarias y eliminadores de formaldehído
CN105431225B (zh)	2013-07-29	2018-06-08	高砂香料工业株式会社	微囊
WO2015130422A1 (fr)	2014-02-28	2015-09-03	Kimberly-Clark Worldwide, Inc.	Produits emballés groupés à ouverture facile
MX2017003966A (es)	2014-09-26	2017-06-30	Procter & Gamble	Composiciones de tratamiento y/o limpieza que comprenden composiciones para reducir el mal olor.
WO2018100411A1 (fr)	2016-11-30	2018-06-07	Arcelormittal	Dispositif de connexion électrique d'installation photovoltaïque

2015
- 2015-09-25 MX MX2017003966A patent/MX2017003966A/es unknown
- 2015-09-25 EP EP15778478.6A patent/EP3197425A1/fr not_active Withdrawn
- 2015-09-25 WO PCT/US2015/052094 patent/WO2016049398A1/fr not_active Application Discontinuation
- 2015-09-25 US US14/865,066 patent/US10113140B2/en active Active
- 2015-09-25 CN CN201580051674.7A patent/CN106687099A/zh active Pending
- 2015-09-25 CN CN201580051685.5A patent/CN106714848A/zh active Pending
- 2015-09-25 MX MX2017003969A patent/MX2017003969A/es unknown
- 2015-09-25 CN CN201580051681.7A patent/CN106716482A/zh active Pending
- 2015-09-25 JP JP2017515909A patent/JP2017530122A/ja not_active Withdrawn
- 2015-09-25 MX MX2017003968A patent/MX2017003968A/es unknown
- 2015-09-25 CA CA2959432A patent/CA2959432A1/fr not_active Abandoned
- 2015-09-25 WO PCT/US2015/052119 patent/WO2016049404A1/fr active Application Filing
- 2015-09-25 MX MX2017003965A patent/MX2017003965A/es unknown
- 2015-09-25 EP EP15778475.2A patent/EP3197423A1/fr not_active Withdrawn
- 2015-09-25 CA CA2960394A patent/CA2960394A1/fr active Pending
- 2015-09-25 US US14/865,010 patent/US20160090556A1/en not_active Abandoned
- 2015-09-25 EP EP15778136.0A patent/EP3197509A1/fr not_active Withdrawn
- 2015-09-25 EP EP15778827.4A patent/EP3197510A1/fr not_active Withdrawn
- 2015-09-25 JP JP2017515904A patent/JP2017531468A/ja active Pending
- 2015-09-25 KR KR1020177006703A patent/KR101971378B1/ko active Active
- 2015-09-25 MX MX2017003971A patent/MX2017003971A/es unknown
- 2015-09-25 AR ARP150103107A patent/AR105148A1/es unknown
- 2015-09-25 MX MX2017003970A patent/MX2017003970A/es unknown
- 2015-09-25 US US14/864,927 patent/US20160089464A1/en not_active Abandoned
- 2015-09-25 MX MX2017003967A patent/MX2017003967A/es unknown
- 2015-09-25 EP EP15781483.1A patent/EP3197426A1/fr not_active Withdrawn
- 2015-09-25 CN CN201580051684.0A patent/CN107073153A/zh active Pending
- 2015-09-25 WO PCT/US2015/052084 patent/WO2016049389A1/fr active Application Filing
- 2015-09-25 US US14/865,412 patent/US20160090558A1/en not_active Abandoned
- 2015-09-25 CA CA2959697A patent/CA2959697A1/fr active Pending
- 2015-09-25 JP JP2017516727A patent/JP2017537173A/ja active Pending
- 2015-09-25 JP JP2017515906A patent/JP2017535628A/ja active Pending
- 2015-09-25 WO PCT/US2015/052219 patent/WO2016049455A1/fr active Application Filing
- 2015-09-25 CA CA2960390A patent/CA2960390A1/fr active Pending
- 2015-09-25 WO PCT/US2015/052225 patent/WO2016049458A1/fr active Application Filing
- 2015-09-25 US US14/865,048 patent/US20160089317A1/en not_active Abandoned
- 2015-09-25 CN CN201580047130.3A patent/CN107001995A/zh active Pending
- 2015-09-25 CN CN201580047110.6A patent/CN106687148A/zh active Pending
- 2015-09-25 CA CA2959546A patent/CA2959546A1/fr not_active Abandoned
- 2015-09-25 WO PCT/US2015/052090 patent/WO2016049395A1/fr active Application Filing
- 2015-09-25 WO PCT/US2015/052130 patent/WO2016049407A1/fr active Application Filing
- 2015-09-25 WO PCT/US2015/052088 patent/WO2016049393A1/fr active Application Filing
- 2015-09-25 EP EP15781212.4A patent/EP3197511A1/fr not_active Withdrawn
- 2015-09-25 US US14/865,056 patent/US20170333591A9/en not_active Abandoned
- 2015-09-25 CA CA2959555A patent/CA2959555A1/fr active Pending
- 2015-09-25 EP EP15775570.3A patent/EP3197507A1/fr not_active Withdrawn
- 2015-09-25 CA CA2959695A patent/CA2959695A1/fr not_active Abandoned
- 2015-09-25 US US14/865,257 patent/US11334694B2/en active Active
- 2015-09-25 US US14/864,973 patent/US20160092661A1/en not_active Abandoned
- 2015-09-25 CA CA2959434A patent/CA2959434C/fr active Active
- 2015-09-25 WO PCT/US2015/052089 patent/WO2016049394A1/fr active Application Filing
- 2015-09-25 US US14/865,099 patent/US20160090557A1/en not_active Abandoned
- 2015-09-25 JP JP2017516708A patent/JP2017537058A/ja active Pending
- 2015-09-25 CN CN201580051700.6A patent/CN106714849A/zh active Pending
- 2015-09-25 CA CA2959691A patent/CA2959691A1/fr not_active Abandoned
- 2015-09-25 CN CN201580051694.4A patent/CN107073154A/zh active Pending
- 2015-09-25 WO PCT/US2015/052092 patent/WO2016049396A1/fr active Application Filing
- 2015-09-25 EP EP15778476.0A patent/EP3197424A1/fr not_active Ceased
- 2015-09-25 EP EP15778137.8A patent/EP3197422A1/fr not_active Withdrawn
- 2015-09-25 US US14/864,994 patent/US20160090555A1/en not_active Abandoned
- 2015-09-25 KR KR1020177006702A patent/KR102008588B1/ko not_active Expired - Fee Related
- 2015-09-25 JP JP2017515907A patent/JP2017531469A/ja active Pending
- 2015-09-25 US US14/865,089 patent/US10552557B2/en active Active
- 2015-09-25 EP EP15775571.1A patent/EP3197508A1/fr not_active Withdrawn
- 2015-09-25 WO PCT/US2015/052093 patent/WO2016049397A1/fr active Application Filing
- 2015-09-25 JP JP2017515911A patent/JP6923439B2/ja active Active
2016
- 2016-06-29 US US15/196,081 patent/US20160306909A1/en not_active Abandoned
2017
- 2017-01-17 US US15/407,477 patent/US20170119917A1/en not_active Abandoned
- 2017-02-01 US US15/421,642 patent/US20170137753A1/en not_active Abandoned
- 2017-02-01 US US15/421,481 patent/US20170137752A1/en not_active Abandoned
- 2017-02-15 US US15/432,957 patent/US20170255725A1/en not_active Abandoned
- 2017-02-27 ZA ZA2017/01449A patent/ZA201701449B/en unknown
- 2017-05-17 US US15/597,376 patent/US20170249407A1/en not_active Abandoned
- 2017-05-17 US US15/597,391 patent/US20170249408A1/en not_active Abandoned
- 2017-09-19 US US15/708,205 patent/US11334695B2/en active Active
- 2017-09-27 US US15/716,544 patent/US20180066210A1/en not_active Abandoned
2019
- 2019-03-26 JP JP2019059135A patent/JP2019162428A/ja active Pending
- 2019-03-27 JP JP2019060537A patent/JP2019123883A/ja active Pending
- 2019-08-02 JP JP2019143148A patent/JP7328058B2/ja active Active

Also Published As

Publication number	Publication date
US20160089317A1 (en)	2016-03-31
US20170249407A1 (en)	2017-08-31
JP2020000884A (ja)	2020-01-09
US20160090556A1 (en)	2016-03-31
CN106714849A (zh)	2017-05-24
US20160092661A1 (en)	2016-03-31
CA2959432A1 (fr)	2016-03-31
AR105148A1 (es)	2017-09-13
US20170255725A1 (en)	2017-09-07
US20180004875A1 (en)	2018-01-04
WO2016049397A1 (fr)	2016-03-31
WO2016049395A1 (fr)	2016-03-31
ZA201701449B (en)	2018-12-19
WO2016049389A1 (fr)	2016-03-31
JP2019123883A (ja)	2019-07-25
MX2017003970A (es)	2017-06-30
WO2016049398A1 (fr)	2016-03-31
US10113140B2 (en)	2018-10-30
MX2017003968A (es)	2017-06-30
MX2017003969A (es)	2017-06-30
MX2017003965A (es)	2017-05-30
MX2017003967A (es)	2017-07-07
KR20170042329A (ko)	2017-04-18
US20170249408A1 (en)	2017-08-31
CN107001995A (zh)	2017-08-01
EP3197425A1 (fr)	2017-08-02
CA2959691A1 (fr)	2016-03-31
EP3197510A1 (fr)	2017-08-02
WO2016049394A1 (fr)	2016-03-31
CN106714848A (zh)	2017-05-24
EP3197426A1 (fr)	2017-08-02
US20160296656A1 (en)	2016-10-13
JP2017531468A (ja)	2017-10-26
US20170137752A1 (en)	2017-05-18
JP2017530122A (ja)	2017-10-12
JP2017531469A (ja)	2017-10-26
KR102008588B1 (ko)	2019-08-07
EP3197422A1 (fr)	2017-08-02
WO2016049396A1 (fr)	2016-03-31
US20160089464A1 (en)	2016-03-31
EP3197507A1 (fr)	2017-08-02
WO2016049407A1 (fr)	2016-03-31
JP2019162428A (ja)	2019-09-26
CA2959434C (fr)	2023-01-10
US20190155975A9 (en)	2019-05-23
US20160089318A1 (en)	2016-03-31
EP3197423A1 (fr)	2017-08-02
KR20170042328A (ko)	2017-04-18
US20180066210A1 (en)	2018-03-08
CN106687099A (zh)	2017-05-17
US20170137753A1 (en)	2017-05-18
CN107073154A (zh)	2017-08-18
JP2017535628A (ja)	2017-11-30
US20160089462A1 (en)	2016-03-31
CN106716482A (zh)	2017-05-24
US20160306909A1 (en)	2016-10-20
JP2017537173A (ja)	2017-12-14
US11334694B2 (en)	2022-05-17
CN107073153A (zh)	2017-08-18
CA2959697A1 (fr)	2016-03-31
EP3197509A1 (fr)	2017-08-02
EP3197508A1 (fr)	2017-08-02
JP2017536859A (ja)	2017-12-14
WO2016049455A1 (fr)	2016-03-31
EP3197511A1 (fr)	2017-08-02
US20160090555A1 (en)	2016-03-31
US20160089465A1 (en)	2016-03-31
US20160090557A1 (en)	2016-03-31
WO2016049458A1 (fr)	2016-03-31
US20170333591A9 (en)	2017-11-23
CA2959434A1 (fr)	2016-03-31
US20170119917A1 (en)	2017-05-04
US20160090558A1 (en)	2016-03-31
WO2016049404A1 (fr)	2016-03-31
MX2017003971A (es)	2017-06-30
CA2960390A1 (fr)	2016-03-31
US11334695B2 (en)	2022-05-17
JP2017537058A (ja)	2017-12-14
MX2017003966A (es)	2017-06-30
WO2016049393A1 (fr)	2016-03-31
US10552557B2 (en)	2020-02-04
CA2959546A1 (fr)	2016-03-31
CA2959555A1 (fr)	2016-03-31
JP6923439B2 (ja)	2021-08-18
CA2960394A1 (fr)	2016-03-31
KR101971378B1 (ko)	2019-04-22
CN106687148A (zh)	2017-05-17
EP3197424A1 (fr)	2017-08-02
JP7328058B2 (ja)	2023-08-16

Publication	Publication Date	Title
CA2959695A1 (fr)	2016-03-31	Substrats contenant des compositions reduisant les mauvaises odeurs
US10240108B2 (en)	2019-03-26	Particles for malodor reduction
KR102584922B1 (ko)	2023-10-04	방향제 조성물
JP2010519368A (ja)	2010-06-03	香料組成物
US10792384B2 (en)	2020-10-06	Rolled fibrous structures comprising encapsulated malodor reduction compositions
EP3325707B1 (fr)	2021-09-29	Compositions pour réduire les mauvaises odeurs et leur utilisation
US20190029928A1 (en)	2019-01-31	Fibrous Structures Comprising Malodor Reduction Compositions
EP4423227A1 (fr)	2024-09-04	Composition de parfum comprenant de l'alpha-guaiène

Legal Events

Date	Code	Title	Description
2017-05-06	EEER	Examination request	Effective date: 20170228
2019-10-28	FZDE	Discontinued	Effective date: 20190916